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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 22459185, 화합물 → HCID 86623474, 화합물

HRID 2176924
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HRID 2176924 반응식
[C:1](OC(=NC1CCCCC1)NC1CCCCC1)([CH3:4])([CH3:3])[CH3:2].[Cl:21][C:22]1[CH:27]=[C:26]([CH2:28][C:29]([OH:31])=[O:30])[CH:25]=[CH:24][N:23]=1>C(Cl)Cl>[Cl:21][C:22]1[CH:27]=[C:26]([CH2:28][C:29]([O:31][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:30])[CH:25]=[CH:24][N:23]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 22459185HCID 22459185, 화합물HCID 24729521(2-Chloropyridin-4-yl)acetic acid

생성물 1

HCID 86623474HCID 86623474, 화합물수율 77%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Compound 2-tert-butyl-1,3-dicyclohexylisourea (650 mg, 2.30 mmol) was added to a solution of 2-(2-chloropyridin-4-yl)acetic acid (200 mg, 1.16 mmol) in DCM (5 ml) at room temperature. The reaction mixture was stirred for 24 h, filtered, washed with DCM (5 ml) and saturated sodium bicarbonate solution (10 ml). The solvent was evaporated in vacuum to afford 200 mg (77%) of tert-butyl 2-(2-chloropyridin-4-yl)acetate as a colorless liquid.

후처리

  1. filtrationfiltered
  2. washwashed with DCM (5 ml) and saturated sodium bicarbonate solution (10 ml)
  3. customThe solvent was evaporated in vacuum

출처 및 근거

ORD 기록
ord-033ca147b90f4b19acc5b650a4a49525
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09067888B2

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