TW432047B - Pyrrolidinyl and pyrrolinyl ethylamine compounds as kappa agonists - Google Patents
Pyrrolidinyl and pyrrolinyl ethylamine compounds as kappa agonists Download PDFInfo
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- TW432047B TW432047B TW086111948A TW86111948A TW432047B TW 432047 B TW432047 B TW 432047B TW 086111948 A TW086111948 A TW 086111948A TW 86111948 A TW86111948 A TW 86111948A TW 432047 B TW432047 B TW 432047B
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Description
101年.03月0'2日修正誉換百 M432047 五、新型說明: 【新型所屬之技術領域】 [0001] 本創作係有關一種光波導組件,尤其涉及一種光波導組 件的定位結構。 【先前技術】 [0002] 於2010年11月02日公告的美國專利第US7, 542, 643B2號 揭示了一種具有固定結構的光波導組件。所述光波導組 件可向前***插座配合,其包括若干光波導及固定光波 導的套管,所述各光波導包括基板、基層、彼此相隔一 定距離排列於基層上的波導核心及包覆於基層與波導核 心的外包層,所述套管設有一個開槽,所述開槽前後方 向貫通,所述光波導堆疊裝置於所述開槽内。然而,此 種製造方法由於係將一層層光波導依序堆疊在套管的一 個開槽内,隨著一層層的公差累積,越上層的光波導, 其沿所述開槽開口方向的正位度影響越大。 [0003] 是以,針對上述問題,有必要對前述套管進行改造。 【新型内容】 [0004] 本創作之目的在於提供一種光波導組件,其對光波導具 有1¾定位精度。 [0005] 為解決前述技術問題,本創作光波導組件可向前***插 座配合,其包括若干光波導及固定光波導的套管,所述 各光波導包括基板、基層、彼此相隔一定距離排列於基 層上的波導核心及包覆於基層與波導核心的外包層,所 述套管設有多個開槽,各開槽前後方向貫通,所述光波 10022267产單編號 A〇101 第3頁/共12頁 1013077521-0 M432047 101年.03月日梭正替换頁 導分成多組並分別堆疊裝置於各開槽内。 [0006] 與先前技術相比,本創作光波導組件具有如下功效: [0007] 所述套管設有多個開槽,各開槽前後方向貫通,所述光 波導分成多組並分別堆疊裝置於各開槽内。這樣設計使 光波導組件在維持相同光波導層數的條件下,減少光波 導的堆疊數量,從而使累積公差縮小,提高定位精度。 [0008] 本新型的其他具體設計如下: [0009] . 其中前述多個開槽包括一個向上側開口的上開槽與一個 向下側開口的下開槽,所述光波導分別豎直方向堆疊設 置於前述上開槽與下開槽。 [0010] 其中前述上開槽與下開槽沿豎直方向對齊。 [0011] 其中前述上下開槽沿水平方向的寬度需較光波導寬度更 寬2〜4微米。 [0012] 其中前述光波導組件還包括設置於上開槽内的光波導上 側的頂蓋與設置於下開槽内的光波導下側的底蓋,用於 壓合光波導。 [0013] 其中前述套管具有設置於上開槽與下開槽之間的分隔壁 、及處於分隔壁水平兩端的定位孔,所述定位孔可與插 座導向配合。 [0014] 其中前述頂蓋與光波導之間、底蓋與光波導之間均具有 預留給固定膠的空間,頂蓋與底蓋是利用固定膠與光波 導黏合。 【實施方式】26#單编號A〇101 第4頁/共12頁 1013077521-0 M432047 1101 年03月 〇·2 [0015] 下面結合附圖來詳細說明本創作之具體實施方式。 [0016] 請參閲第一圖及第四圖所示,本創作係一種光波導組件 100,其可向前***插座配合,所述光波導組件10()包括 若干光波導140、固定光波導140的套管110以及用於壓 合光波導140的頂蓋120與底蓋13〇,所述各光波導140包 括基板141、基層143、波導核心142及外包層144,所述 波導核心142彼此相隔一定距離排列於基層143上,所述 外包層144熔於基層143從而包覆於波導核心142 ^所述 套官110設有兩個開槽、設置於兩個開槽之間的分隔壁 111及處於分隔壁111水平兩端的定位孔112,所述定位 孔112可與插座導向配合。所述套管11〇包括一個向上侧 開口的上開槽14 6與一個向下側開口的下開槽14 7,所述 上開槽14 6與下開槽14 7沿豎直方向對齊,各開槽前後方 向貫通,所述上下開槽沿水平方向的寬度需較光波導14〇 寬度更寬2>·4微米。所述光波導14〇分別豎直方向堆疊設 置於前述上開槽146與下開槽147。所述頂蓋120設置於 上開槽146内光波導140的上側,所述底蓋13〇設置於下 開槽147内光波導140的下側’所述頂蓋12〇與底蓋130用 於壓合光波導14(^所述頂蓋120與光波導14〇之間、底 蓋130與光波導140之間均具有預留給固定膠丨45的空間, 頂蓋120與底蓋130是利用固定膠145與光波導140黏合。 [00Π] 综上所述,本創作確已符合新型專利之要件,爰依法提 出專利申請》惟,以上所述者僅係本創作之較佳實施方 式,本創作之範圍並不以上述實施方式爲限,舉凡熟習 本案技藝之人士援依本創作之精神所作之等效修飾或變 10022267产單編號 A0101 第5頁/共12頁 1013077521-0 M432047 101年03月0>日核正替換頁 化,皆應涵以下申請專利範圍内。 【圖式簡單說明】 [0018] 第一圖係符合本發明的一種光波導組件的立體圖。 [0019] 第二圖係第一圖中光波導組件的立體***圖。 [0020] 第三圖係第一圖中光波導組件的前視圖。 [0021] 第四圖係第二圖中套管的立體圖。 【主要元件符號說明】 [0022] 光波導組件100 · [0023] 套管 1 1 0 [0024] 分隔壁111 [0025] 定位孔112 [0026] 頂蓋 120 [0027] 底蓋 130 [0028] 光波導 140 # [0029] 基板 141 [0030] 波導核心142 - [0031] 基層 143 [0032] 外包層144 [0033] 固定膠145 [0034] 上開槽146 10〇222^科號删1 第6頁/共12頁 1013077521-0 M432047 [0035] 下開槽147 101年.03月的日梭正替&頁
1〇〇2226#料號删1 第7頁/共12頁 1013077521-0 Μ432^,^^ . 200222678 _____ ※記號部分請勿填寫 ※申請案號:100222678 ※申請日:/"6^. Q 一、新型名稱: 寬專收字第:1013〇77521- .1〇1年.03月0>日按正_頁 丨__ 舰日 ^IPC^: (2006.01) Ο 光波導組件
OPTICAL WAVEGUIDE ASSEMBLY 二、中文新型摘要: 本創作係提供一種光波導組件,可向前***插座配合,其包 括若干光波導及固定光波導的套管,所述各光波導包括基板 、基層、彼此相隔一定距離排列於基層上的波導核心及包覆 於基層與波導核心的外包層,所述套管設有多個開槽,各開 槽前後方向貫通,所述光波導分成多組並分別堆疊裝置於各 開槽内。 三、英文新型摘要:
An optical waveguide assembly used for mating forwardly into a socket, includes a number of optical waveguides and a ferrule which receiving the optical waveguides, Each of the optical waveguides includes a substrate, a base layer, a number of waveguide cores arraying on the base layer and a clad layer covering the base layer and the waveguide cores. The ferrule defines a number of slots, extending there through forwardly .The optical waveguides are divided into a number of groups and each group of the optical waveguides is stacked in corresponding slot. 10022267#單編號 A0101 第1頁/共12頁 1013077521-0 M432047 _ 101年.03月0乏日按正替換頁 六、申請專利範圍: 1 · 一種光波導組件,可向前***插座配合,其包括若干光波 導及固定光波導的套管,所述各光波導包括基層、壓合於 基層上的基板、彼此相隔一定距離排列於基層上的波導核 心及包覆於基層與波導核心的外包層,其特徵在於:所述 •套管設有多個開槽,各開槽前後方向貫通,所述光波導分 成多組並分別堆疊裝置於各開槽内。 2.如申請專利範圍第丨項所述之光波導組件,其中前述多個 開槽包括一個向上側開口的上開槽與一個向下側開口的下 開槽,所述光波導分別豎直方向堆疊設置於前述上開槽與 · 下開槽。 3 .如申請專利範圍第2項所述之光波導組件,其中前述上開 槽與下開槽沿豎直方向對齊。 4 .如申請專利範圍第2項所述之光波導組件,其中前述上下 開槽沿水平方向的寬度需較光波導寬度更寬微米。 5 .如申請專利範圍第2項所述之光波導組件,其中前述光波 導組件還包括設置於上開槽内的光波導上側的頂蓋與設置 於下開槽内的光波導下側的底蓋,用於壓合光波導。 ^ 6 ·如申請專利範圍第2項所述之光波導組件,其中前述套管 具有δ又置於上開槽與下開槽之間的分隔壁、及處於分隔壁 水平兩端的定位孔,所述定位孔可與插座導向配合。 7 ·如申請專利範圍第5項所述之光波導組件,其中前述頂蓋 與光波導之間、底蓋與光波導之間均具有預留給固定膠的 空間,頂蓋與底蓋是利用固定膠與光波導黏合。 1〇〇22267卢單編號 Α0101 第8頁/共12頁 1013077521-0
Viol 棱正 m^〇A1 七、®式·
1〇13〇^521 第9 $ 兵 12育 M432047 101年.03月02日修正替換頁
1013077521-0 M432047
10022267产概 Α〇101 101年.03月02日修正替換頁
第二圖 第11頁/共12頁 1013077521-0 M432047 101年.03月0乏日核正替換頁 ⑽22267#單编號
第四圖 第12頁/共12頁
1013077521-0 M432047 101年03月02日修正替換頁 四、指定代表圖: (一) 本案指定代表圖為:第(三)圖 (二) 本代表圖之元件符號簡單說明: 套管:110 分隔壁:111 定位孔:112 基板:141 基層:143 外包層:14 4 波導核心:142 ^ 固定膠:145 10022267#單编號 A〇101 第2頁/共12頁 1013077521-0
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WO1999051587A1 (fr) | 1998-04-01 | 1999-10-14 | Ono Pharmaceutical Co., Ltd. | Derives de thiophene condenses et medicaments contenant ceux-ci comme principe actif |
EP0982297A3 (en) * | 1998-08-24 | 2001-08-01 | Pfizer Products Inc. | Process for the preparation of hydroxy-pyrrolidinyl hydroxamic acid derivatives being opioid kappa receptor agonists |
AU2002247886A1 (en) * | 2001-04-30 | 2002-11-11 | Pfizer Products Inc. | Process for preparing hydroxypyrrolidinyl ethylamine compounds useful as kappa agonists |
WO2003072544A1 (en) * | 2002-02-28 | 2003-09-04 | Pfizer Products Inc. | Crystalline anhydrous and monohydrate benzoate salts of (2's,3s)-3-hydroxy-n-{2{n-methyl-n-4-(n-propylamino-carbonyl)phenyl]amino-2-phenyl}-ethylpyrrolidine |
AU2003269399A1 (en) * | 2002-11-01 | 2004-05-25 | Pfizer Products Inc. | Process for the preparation of pyrrolidinyl ethylamine compounds via a copper-mediated aryl amination |
CN1972914A (zh) * | 2004-03-31 | 2007-05-30 | 詹森药业有限公司 | 作为组胺h3受体配合体的非咪唑杂环化合物 |
US7746514B2 (en) * | 2004-04-14 | 2010-06-29 | Hung-Yi Hsu | Scanner and exposure control method thereof |
US20070213319A1 (en) * | 2006-01-11 | 2007-09-13 | Angion Biomedica Corporation | Modulators of hepatocyte growth factor/c-Met activity |
CA2653940C (en) | 2006-05-30 | 2015-07-14 | Janssen Pharmaceutica N.V. | Substituted pyridyl amide compounds as modulators of the histamine h3 receptor |
CN101511807A (zh) * | 2006-06-29 | 2009-08-19 | 詹森药业有限公司 | 组胺h3受体的取代的苯甲酰胺调节剂 |
CN105712977B (zh) | 2007-11-20 | 2021-06-29 | 詹森药业有限公司 | 作为组胺h3受体调节剂的环烷基氧基吡啶化合物和杂环烷基氧基吡啶化合物 |
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GB8801304D0 (en) | 1988-01-21 | 1988-02-17 | Ici Plc | Diamine compounds |
DE4034785A1 (de) * | 1990-11-02 | 1992-05-07 | Merck Patent Gmbh | 1-(2-arylethyl)-pyrrolidine |
DE3935371A1 (de) | 1988-12-23 | 1990-07-05 | Merck Patent Gmbh | Stickstoffhaltige ringverbindungen |
US5232978A (en) * | 1988-12-23 | 1993-08-03 | Merck Patent Gesellschaft Mit Beschrankter Haftung | 1-(2-arylethyl)-pyrrolidines |
WO1994018165A1 (en) | 1993-02-12 | 1994-08-18 | Pfizer Inc. | Sulfonamide compounds as opioid k-receptor agonists |
IL117440A0 (en) * | 1995-03-31 | 1996-07-23 | Pfizer | Pyrrolidinyl hydroxamic acid compounds and their production process |
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