Dimethyl Sulfoxide → 3-(6-carboxyhex-1-enyl)-N-(3-pyridyl)indole

HRID 485346노트

반응식

HRID 485346 반응식
CS(C)=O.C([Li])CCC.[Br-].[C:11]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([OH:13])=[O:12].[N:38]1[CH:43]=[CH:42][CH:41]=[C:40]([N:44]2[C:52]3[C:47](=[CH:48][CH:49]=[CH:50][CH:51]=3)[C:46]([CH:53]=O)=[CH:45]2)[CH:39]=1>O>[C:11]([CH2:14][CH2:15][CH2:16][CH2:17][CH:18]=[CH:53][C:46]1[C:47]2[C:52](=[CH:51][CH:50]=[CH:49][CH:48]=2)[N:44]([C:40]2[CH:39]=[N:38][CH:43]=[CH:42][CH:41]=2)[CH:45]=1)([OH:13])=[O:12]

참가 물질

6

실험 절차

A solution of dimsyllithium (from 80 ml of dimethylsulfoxide and 13 ml of 2.1M n-butyllithium) is stirred under nitrogen at room temperature, and 6.2 g of 5-carboxypentyltriphenylphosphonium bromide is added in portions. The reaction mixture is stirred for 30 minutes and 3.0 g of N-(3-pyridyl)indole-3-carboxaldehyde is added. After 18 hours at room temperature, the reaction mixture is diluted with 240 ml of water and extracted with 100 ml of ethyl acetate. The aqueous phase is neutralized with 1.1 ml of concentrated hydrochloric acid and extracted with ethyl acetate. The extracts are dried over sodium sulfate and evaporated to an oil which is triturated with ether to give a semi-solid which is recrystallized from methanol to yield 3-(6-carboxyhex-1-enyl)-N-(3-pyridyl)indole, m.p. 124°-125°.

후처리

  1. waitAfter 18 hours at room temperature
  2. extractionextracted with 100 ml of ethyl acetate
  3. extractionextracted with ethyl acetate
  4. dry with materialThe extracts are dried over sodium sulfate
  5. customevaporated to an oil which
  6. customis triturated with ether
  7. customto give a semi-solid which
  8. customis recrystallized from methanol

출처 및 근거

ORD 기록
ord-2dc8df6ce6464c01b10bdb1e35513d3e
출처 데이터셋
uspto-grants-1985_08
특허 번호
US04536505

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