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Methyl 3-benzyloxycarbonylamino-4-(1-pentynyl)benzoate → HCID 53794293, 화합물

HRID 1108678
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HRID 1108678 반응식
[CH2:1]([O:8][C:9]([NH:11][C:12]1[CH:13]=[C:14]([CH:19]=[CH:20][C:21]=1[C:22]#[C:23][CH2:24][CH2:25][CH3:26])[C:15]([O:17][CH3:18])=[O:16])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>O1CCCC1.[Cl-].[Na+].[Au+3].[Cl-].[Cl-].[Cl-]>[CH2:1]([O:8][C:9]([N:11]1[C:12]2[C:21](=[CH:20][CH:19]=[C:14]([C:15]([O:17][CH3:18])=[O:16])[CH:13]=2)[CH:22]=[C:23]1[CH2:24][CH2:25][CH3:26])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 22627418Methyl 3-benzyloxycarbonylamino-4-(1-pentynyl)benzoate

생성물 1

HCID 53794293HCID 53794293, 화합물수율 89.8%

시약·촉매·용매 2

HCID 9928900AuCl4Na촉매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of methyl 3-benzyloxycarbonylamino-4-(1-pentynyl)benzoate (949 mg) in tetrahydrofuran (24 ml) was added gold(III)sodium chloride (24 mg) under argon atmosphere, and the mixture was heated under reflux for 100 minutes. The solvent was evaporated in vacuo and the residue was chromatographed on silica gel eluting with a mixture of hexane, dichloromethane, and ethyl acetate (6:3:2) to give methyl 1-benzyloxycarbonyl-2-propylindole-6-carboxylate (852 mg) as colorless crystals.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 100 minutes
  3. customThe solvent was evaporated in vacuo
  4. customthe residue was chromatographed on silica gel eluting with a mixture of hexane, dichloromethane, and ethyl acetate (6:3:2)

출처 및 근거

ORD 기록
ord-b1157839ecbd4d4594b3d7f08fa1c45e
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06069156

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