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Ammonia → 4-amino-N,1-dimethyl-2-oxo-3-pentenesulfonamide

HRID 1252255
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HRID 1252255 반응식
[NH3:1].[CH3:2][N:3]1[C:8]([CH3:9])=[CH:7][C:6](=[O:10])[CH:5]([CH3:11])[S:4]1(=[O:13])=[O:12]>CO>[NH2:1][C:8]([CH3:9])=[CH:7][C:6](=[O:10])[CH:5]([CH3:11])[S:4]([NH:3][CH3:2])(=[O:13])=[O:12]
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 201410512,3,6-trimethyl-2H-1,2-thiazin-5(6H)-one 1,1-dioxide

생성물 1

HCID 867421514-amino-N,1-dimethyl-2-oxo-3-pentenesulfonamide

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A moderately rapid stream of dry ammonia was introduced at 20°-25° during 3 hours into a solution of 2.5 g of 2,3,6-trimethyl-2H-1,2-thiazin-5(6H)-one 1,1-dioxide in 25 ml of methanol and the mixture was thereupon left to stand overnight. The dark yellow solution obtained was concentrated to dryness under reduced pressure and the crystalline residue was recrystallized from ethanol. There were obtained 2.3 g of 4-amino-N,1-dimethyl-2-oxo-3-pentenesulfonamide in the form of colorless crystals, m.p. 140°-143°.

후처리

  1. waitthe mixture was thereupon left
  2. customThe dark yellow solution obtained
  3. concentrationwas concentrated to dryness under reduced pressure
  4. customthe crystalline residue was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-7c664e08997b42b489d60152ce5b2e87
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04742069

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