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Carbon tetrabromide → 5-Fluoro-indolyl-3-propylbromide

HRID 1954221
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반응식

HRID 1954221 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2CCCO.[C:15]([Br:19])(Br)(Br)Br.[C:20]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=C[CH:21]=1>C(Cl)Cl>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([CH:15]([Br:19])[CH2:20][CH3:21])=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 150205413-(5-fluoro-1H-indol-3-yl)propan-1-ol2회

생성물 1

HCID 540585145-Fluoro-indolyl-3-propylbromide수율 99%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 3-(5-fluoro-1H-indol-3-yl)-propan-1-ol (Intermediate 6) prepared in accordance with the procedures set forth in Demerson et al., J. Med. Chem., 19:391-395 (1976). (25.4 g, 0.13 mol), carbon tetrabromide (65.5 g, 0.2 mol) and triphenylphosphine (52 g, 0.2 mol) in methylene chloride (156 ml) was allowed to stir for 2 hours. The solvent was evaporated and the product chromatographed (30% ethyl acetate-hexanes) to afford 33.5 g (99%) of product.

후처리

  1. customThe solvent was evaporated
  2. customthe product chromatographed (30% ethyl acetate-hexanes)

출처 및 근거

ORD 기록
ord-d4053f703fe24a289bfd1acf2f51dd38
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06121307

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