3-(Trifluoromethyl)benzaldehyde → 3-[(1,3-Benzodithiol-2-ylidene)amino]-2-thioxo-5-[[3-(trifluoromethyl)phenyl]methylene]-4-thiazolidinone

HRID 2419145노트

반응식

HRID 2419145 반응식
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[S:3][C:2]1=[N:10][N:11]1[C:15](=[O:16])[CH2:14][S:13][C:12]1=[S:17].[F:18][C:19]([F:29])([F:28])[C:20]1[CH:21]=[C:22]([CH:25]=[CH:26][CH:27]=1)[CH:23]=O.C(O)(=O)C.N1CCCCC1>C(COC)OC.ClCCl>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[S:3][C:2]1=[N:10][N:11]1[C:15](=[O:16])[C:14](=[CH:23][C:22]2[CH:25]=[CH:26][CH:27]=[C:20]([C:19]([F:18])([F:28])[F:29])[CH:21]=2)[S:13][C:12]1=[S:17]

참가 물질

6

실험 절차

A slurry of 3-[(1,3-benzodithiol-2-ylidene)amino]-2-thioxo-4-thiazolidinone (see example 37), m-trifluoromethylbenzaldehyde (10 ml, excess) and acetic acid/piperidine (1 ml) in 250 ml of anhydrous glyme is heated at reflux for 7 days. The reaction mixture is concentrated in vacuo and the oily residue extracted with hexane. The solid thus obtained is slurried in 1000 ml of dichloromethane and stirred at room temperature overnight. The slurry is filtered and the filtrate concentrated in vacuo. The solid residue thus obtained is recrystallized from dimethylformamide to yield 500 mg of the title compound, melting point 268°-269° C.

후처리

  1. temperatureat reflux for 7 days
  2. concentrationThe reaction mixture is concentrated in vacuo
  3. extractionthe oily residue extracted with hexane
  4. customThe solid thus obtained
  5. filtrationThe slurry is filtered
  6. concentrationthe filtrate concentrated in vacuo
  7. customThe solid residue thus obtained
  8. customis recrystallized from dimethylformamide

출처 및 근거

ORD 기록
ord-6aae0c0ec5a948ac9bee6e3d81d23ffc
출처 데이터셋
uspto-grants-1978_08
특허 번호
US04104467

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