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Dimethylformamide → HCID 53748727, 화합물

HRID 437712
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HRID 437712 반응식
CS(Cl)(=O)=O.[NH2:6][C:7]1[S:11][N:10]=[C:9]([O:12][CH2:13][CH2:14][CH3:15])[C:8]=1[C:16]#[N:17].[CH3:18][N:19]([CH3:22])[CH:20]=O>>[C:16]([C:8]1[C:9]([O:12][CH2:13][CH2:14][CH3:15])=[N:10][S:11][C:7]=1[N:6]=[CH:18][N:19]([CH3:22])[CH3:20])#[N:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6228DimethylformamideHCID 31297Methanesulfonyl chlorideHCID 21396807HCID 21396807, 화합물

생성물 1

HCID 53748727HCID 53748727, 화합물

실험 절차

A mixture of 13.7 g of methanesulfonyl chloride in 25 ml of dimethylformamide was stirred at room temperature for about 16 hours. Into the mixture was stirred 11 g of 5-amino-4-cyano-3-propoxyisothiazole which addition caused an exothermic reaction. The mixture was concentrated under reduced pressure and the residue was recrystallized from ethanol to give 2.7 g of crystalline N'-(4-cyano-3-propoxy-5-isothiazolyl)-N,N-dimethylformamidine, m.p. 117°-118°. The nmr spectrum was consistent with the assigned structure.

후처리

  1. stirringInto the mixture was stirred
  2. customan exothermic reaction
  3. concentrationThe mixture was concentrated under reduced pressure
  4. customthe residue was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-f2e3cd44ec96400ebcb60793fac6d257
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04032322

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