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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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tert-butyl N-(1-carbamothioylpiperidin-4-yl)carbamate → Ethyl 2-(4-aminopiperidin-1-yl)-4-[(2-methoxyethoxy)methyl]-1,3-thiazole-5-carboxylate hydrochloride

HRID 2233892
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HRID 2233892 반응식
[NH2:1][C:2]([N:4]1[CH2:9][CH2:8][CH:7]([NH:10]C(=O)OC(C)(C)C)[CH2:6][CH2:5]1)=[S:3].[Cl:18][CH:19]([C:25](=O)[CH2:26][O:27][CH2:28][CH2:29][O:30][CH3:31])[C:20]([O:22][CH2:23][CH3:24])=[O:21]>CCO>[ClH:18].[NH2:10][CH:7]1[CH2:6][CH2:5][N:4]([C:2]2[S:3][C:19]([C:20]([O:22][CH2:23][CH3:24])=[O:21])=[C:25]([CH2:26][O:27][CH2:28][CH2:29][O:30][CH3:31])[N:1]=2)[CH2:9][CH2:8]1
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참가 물질

4

반응물 2

HCID 59296117tert-butyl N-(1-carbamothioylpiperidin-4-yl)carbamate2회HCID 86038328Ethyl 2-chloro-4-(2-methoxyethoxy)-3-oxobutanoate2회

생성물 1

HCID 68579915Ethyl 2-(4-aminopiperidin-1-yl)-4-[(2-methoxyethoxy)methyl]-1,3-thiazole-5-carboxylate hydrochloride

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
90 °C

실험 절차

tert-Butyl [1-(aminocarbonothioyl)piperidin-4-yl]carbamate (Intermediate 125, 400 mg) was dissolved in anhydrous EtOH (5 ml). Ethyl 2-chloro-4-(2-methoxyethoxy)-3-oxobutanoate (Intermediate 124, 368 mg) was added and the mixture was heated at 90° C. for 18 h. Partial removal of Boc group was detected. Solvent was removed in vacuo and the dried material was treated with 4 N HCl/dioxane for 2 h. Solvent was removed in vacuo to give a brown/yellow solid which was dried to afford the title compound which was used without further purification (508 mg).

후처리

  1. customPartial removal of Boc group
  2. customSolvent was removed in vacuo
  3. additionthe dried material was treated with 4 N HCl/dioxane for 2 h
  4. customSolvent was removed in vacuo
  5. customto give a brown/yellow solid which
  6. customwas dried

출처 및 근거

ORD 기록
ord-61cbc8f42d5c4c0ba076f7bea15964eb
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709503B2

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