Dichloromethane → HCID 14769542, 화합물

HRID 1381343노트

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HRID 1381343 반응식
[CH:1]([NH:3][C:4]1[S:8][N:7]=[C:6]([C:9]([O:11]C)=O)[N:5]=1)=[O:2].[CH3:13][S:14][CH2:15][S:16]([CH3:18])=[O:17].[H-].[Na+].C(Cl)Cl>CN(C)C=O>[CH:1]([NH:3][C:4]1[S:8][N:7]=[C:6]([C:9](=[O:11])[CH:15]([S:14][CH3:13])[S:16]([CH3:18])=[O:17])[N:5]=1)=[O:2]

참가 물질

6

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온도
40 °C

실험 절차

To a mixture of methyl 5-formamido-1,2,4-thiadiazole-3-carboxylate (9.2 g) and methyl methylthiomethyl sulfoxide (6.1 g) in N,N-dimethylformamide (100 ml) was added 50% sodium hydride (7.1 g) with cooling in an ice-bath. The mixture was stirred for an hour at ambient temperature and for an additional one hour at 40° C. After cooling to ambient temperature, methylene chloride (300 ml) was added to the reaction mixture, and the resulting precipitates were collected by filtration and washed with methylene chloride. The precipitates were added to a stirred mixture of hydrochloric acid (14.7 ml), ice-water (200 ml) and methylene chloride (200 ml). An insoluble material was filtered off and the methylene chloride layer was separated from the filtrate. The solution was dried over anhydrous magnesium sulfate, evaporated and the residue was triturated with diethyl ether to give the title compound (4.5 g), mp. 130° to 132° C.

후처리

  1. temperaturewith cooling in an ice-bath
  2. temperatureAfter cooling to ambient temperature
  3. customthe resulting precipitates
  4. filtrationwere collected by filtration
  5. washwashed with methylene chloride
  6. additionThe precipitates were added to a stirred mixture of hydrochloric acid (14.7 ml), ice-water (200 ml) and methylene chloride (200 ml)
  7. filtrationAn insoluble material was filtered off
  8. customthe methylene chloride layer was separated from the filtrate
  9. dry with materialThe solution was dried over anhydrous magnesium sulfate
  10. customevaporated
  11. customthe residue was triturated with diethyl ether

출처 및 근거

ORD 기록
ord-fd540f6546c944d8bcd307f2cc754d4e
출처 데이터셋
uspto-grants-1986_04
특허 번호
US04585872

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