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Benzyl Bromide → 3-(1,4-Dioxa-spiro[4,5]dec-8-yl)-5-cyano-1-benzyl-indole

HRID 428510
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인쇄 미리보기

반응식

HRID 428510 반응식
[O:1]1[C:5]2([CH2:10][CH2:9][CH:8]([C:11]3[C:19]4[C:14](=[CH:15][CH:16]=[C:17]([C:20]#[N:21])[CH:18]=4)[N:13]([CH2:22][CH3:23])[CH:12]=3)[CH2:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.C(Br)[C:25]1[CH:30]=[CH:29]C=[CH:27][CH:26]=1>>[O:4]1[C:5]2([CH2:10][CH2:9][CH:8]([C:11]3[C:19]4[C:14](=[CH:15][CH:16]=[C:17]([C:20]#[N:21])[CH:18]=4)[N:13]([CH2:22][C:23]4[CH:29]=[CH:30][CH:25]=[CH:26][CH:27]=4)[CH:12]=3)[CH2:7][CH2:6]2)[O:1][CH2:2][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7498Benzyl BromideHCID 184140623-(1,4-Dioxa-spiro[4,5]dec-8-yl)-5-cyano-1-ethyl-indole

생성물 1

HCID 184141213-(1,4-Dioxa-spiro[4,5]dec-8-yl)-5-cyano-1-benzyl-indole수율 57%

실험 절차

This compound was prepared in the manner described above for intermediate 5b by replacing ethylbromide with benzylbromide (14.3 g, 84 mmol) to afford 6.04 g (57%) of the title compound as a white solid: mp 129-130° C.

후처리

  1. customThis compound was prepared in the manner

출처 및 근거

ORD 기록
ord-c009ef33481c4c518e9748598561d70c
출처 데이터셋
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06313126B1

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