Citric Acid → HCID 69487009, 화합물

HRID 1271844노트

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HRID 1271844 반응식
[C:1]([O:5][C:6]([NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[NH:15][C:16]([C:18]1[S:22][C:21]2[CH:23]=[CH:24][C:25]([O:27]C(=O)C3C=CC=CC=3)=[CH:26][C:20]=2[CH:19]=1)=[O:17])=[O:7])([CH3:4])([CH3:3])[CH3:2].C[O-].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CO>[C:1]([O:5][C:6](=[O:7])[NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[NH:15][C:16]([C:18]1[S:22][C:21]2[CH:23]=[CH:24][C:25]([OH:27])=[CH:26][C:20]=2[CH:19]=1)=[O:17])([CH3:4])([CH3:2])[CH3:3]

참가 물질

5

반응물 3

HCID 311Citric AcidHCID 10942334Sodium MethoxideHCID 86760485HCID 86760485, 화합물

생성물 1

HCID 69487009HCID 69487009, 화합물

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a suspension of 732 mg (1.5 mmol) benzoic acid 2-(2-tert-butoxycarbonylamino-phenylcarbamoyl)-benzo[b]thiophen-5-yl ester (3) in 30 ml methanol was added 1.0 ml of a 5.4M solution of NaOMe in methanol. After 3 h at room temperature the reaction solution was poured on 5% aqueous citric acid. Extraction with ethyl acetate, washing of the organic phase with brine. The organic phase was dried over sodium sulfate, the solvent was evaporated and the residue subjected to silica gel chromatography (petrolether/ethyl acetate 3:1). {2-[(5-Hydroxy-benzo[b]thiophene-2-carbonyl)-amino]-phenyl}-carbamic acid tert-butyl ester (4) was recrystallized from ethyl acetate/diethyl ether to yield 546 mg (1.42 mmol) as colorless crystals, mp. 185° C. (decomp.).

후처리

  1. extractionExtraction with ethyl acetate
  2. washwashing of the organic phase with brine
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. customthe solvent was evaporated
  5. custom{2-[(5-Hydroxy-benzo[b]thiophene-2-carbonyl)-amino]-phenyl}-carbamic acid tert-butyl ester (4) was recrystallized from ethyl acetate/diethyl ether
  6. customto yield 546 mg (1.42 mmol) as colorless crystals, mp. 185° C. (decomp.)

출처 및 근거

ORD 기록
ord-71b8f13f79894337a342dfe59a1ba393
출처 데이터셋
uspto-grants-2007_04
특허 번호
US07208491B2

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