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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 178472741, 화합물 → HCID 178525874, 화합물

HRID 402525
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HRID 402525 반응식
C([O:3][C:4](=[O:26])[CH2:5][NH:6][C@H:7]1[CH2:12][CH2:11][C@@H:10]([O:13][C:14]2[CH:15]=[C:16]3[C:21](=[CH:22][C:23]=2[Cl:24])[C:20](=[O:25])[NH:19][CH:18]=[CH:17]3)[CH2:9][CH2:8]1)C>CO>[Cl:24][C:23]1[CH:22]=[C:21]2[C:16]([CH:17]=[CH:18][NH:19][C:20]2=[O:25])=[CH:15][C:14]=1[O:13][C@@H:10]1[CH2:9][CH2:8][C@H:7]([NH:6][CH2:5][C:4]([OH:26])=[O:3])[CH2:12][CH2:11]1
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참가 물질

3

반응물 1

HCID 178472741HCID 178472741, 화합물

생성물 1

HCID 178525874HCID 178525874, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

185 mg of [4-(7-chloro-1-oxo-1,2-dihydro-isoquinolin-6-yloxy)-cis-cyclohexylamino]-acetic acid ethyl ester (23, crude product) were dissolved in 2 ml methanol. After adding 2 ml of 2 N NaCO3-solution, the solution was stirred at room temperature for 1.5 h. The solvent was evaporated in vacuo and the residue was purified by preparative HPLC, which delivers the title compound as trifluoro acetate. Rt=0.91 min (Method B). Detected mass: 351.3 (M+H+).

후처리

  1. customThe solvent was evaporated in vacuo
  2. customthe residue was purified by preparative HPLC, which

출처 및 근거

ORD 기록
ord-244dcbaebdd54a9f84f7202000da47c1
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08742116B2

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