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Chlorosulfonyl isocyanate → 3-Cyano-1-cyclopropyl-6-methoxyindole

HRID 1009640
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인쇄 미리보기

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HRID 1009640 반응식
[CH:1]1([N:4]2[C:12]3[C:7](=[CH:8][CH:9]=[C:10]([O:13][CH3:14])[CH:11]=3)[CH:6]=[CH:5]2)[CH2:3][CH2:2]1.ClS([N:19]=[C:20]=O)(=O)=O>CN(C=O)C>[C:20]([C:6]1[C:7]2[C:12](=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=2)[N:4]([CH:1]2[CH2:3][CH2:2]2)[CH:5]=1)#[N:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70918Chlorosulfonyl isocyanateHCID 594305841-Cyclopropyl-6-methoxylindole

생성물 1

HCID 594252703-Cyano-1-cyclopropyl-6-methoxyindole수율 82%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 1-cyclopropyl-6-methoxylindole (3.29 g, 17.6 mmol) in dry DMF (30 mL), at 0° C., is added chlorosulfonyl isocyanate (3.11 g, 1.91 mL, 22.0 mmol). After the addition, the mixture is stirred at room temperature for 2 h, followed by aqueous work-up. Chromatography (silica gel, hexanes/EtOAc, 9/1) furnishes 3-cyano-1-cyclopropyl-6-methoxyindole (3.05 g, 82%).

후처리

  1. additionAfter the addition

출처 및 근거

ORD 기록
ord-6528acfec6bc47e6812c9c3ec9b0edd0
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07973069B2

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