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Ammonia → HCID 90202338, 화합물

HRID 929761
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HRID 929761 반응식
C([O:3][C:4]([C:6]1[O:10][N:9]=[C:8]([C:11]2[CH:16]=[CH:15][C:14]([O:17][Si:18]([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19])=[CH:13][CH:12]=2)[CH:7]=1)=O)C.[NH3:25]>CCO>[C:21]([Si:18]([CH3:20])([CH3:19])[O:17][C:14]1[CH:15]=[CH:16][C:11]([C:8]2[CH:7]=[C:6]([C:4]([NH2:25])=[O:3])[O:10][N:9]=2)=[CH:12][CH:13]=1)([CH3:24])([CH3:23])[CH3:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 90202312HCID 90202312, 화합물2회

생성물 1

HCID 90202338HCID 90202338, 화합물수율 35%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-isoxazole-5-carboxylic acid ethyl ester (which may be prepared as described in Preparation of Intermediate 12; 500 mg, 1.4 mmol) was dissolved in a saturated solution of NH3 in EtOH (200 mL). The mixture was stirred at room temperature for 60 h. The solvent was evaporated and the residue was purified by chromatography (50-60% EtOAc/hexanes) to give 3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-isoxazole-5-carboxylic acid amide (160 mg, 35%) as a white solid.

후처리

  1. customThe solvent was evaporated
  2. customthe residue was purified by chromatography (50-60% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-4e2067b3cda24e679e0448a4335c9b96
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09296711B2

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