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Lithium Hydroxide → (5-{2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-cyano-phenyl}-pyridin-3-yl)-acetic acid

HRID 554593
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반응식

HRID 554593 반응식
C([O:3][C:4](=[O:34])[CH2:5][C:6]1[CH:7]=[N:8][CH:9]=[C:10]([C:12]2[CH:17]=[CH:16][C:15]([C:18]#[N:19])=[CH:14][C:13]=2[CH2:20][N:21]([CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[C:22]([CH:24]2[CH2:26][CH2:25]2)=[O:23])[CH:11]=1)C.[Li+].[OH-]>CO>[CH2:27]([N:21]([CH2:20][C:13]1[CH:14]=[C:15]([C:18]#[N:19])[CH:16]=[CH:17][C:12]=1[C:10]1[CH:11]=[C:6]([CH2:5][C:4]([OH:34])=[O:3])[CH:7]=[N:8][CH:9]=1)[C:22]([CH:24]1[CH2:26][CH2:25]1)=[O:23])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 67212964(5-{2-[(Benzyl-cyclopropanecarbonyl-amino)-methyl]-4-cyano-phenyl}-pyridin-3-yl)-acetic acid ethyl ester

생성물 1

HCID 45138331(5-{2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-cyano-phenyl}-pyridin-3-yl)-acetic acid

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

(5-{2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-cyano-phenyl}-pyridin-3-yl)-acetic acid ethyl ester (0.1 g, 0.22 mmol) was dissolved in MeOH (10 mL) and treated with 1N aqueous LiOH (1 mL) dropwise. The reaction was stirred at room temperature for 1 hour, and then quenched with 1N aqueous HCl (1 ml) and extracted with EtOAc. The combined organic layers were dried and concentrated to give Compound 3.

후처리

  1. customquenched with 1N aqueous HCl (1 ml)
  2. extractionextracted with EtOAc
  3. customThe combined organic layers were dried
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a707b20cdedd4a61b8b14903d25fa45a
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08049015B2

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