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Ammonia → Methyl 5-sulfamoyl-1,3-thiazole-4-carboxylate

HRID 2073697
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HRID 2073697 반응식
Cl[S:2]([C:5]1[S:9][CH:8]=[N:7][C:6]=1[C:10]([O:12][CH3:13])=[O:11])(=[O:4])=[O:3].[NH3:14]>O1CCCC1>[NH2:14][S:2]([C:5]1[S:9][CH:8]=[N:7][C:6]=1[C:10]([O:12][CH3:13])=[O:11])(=[O:4])=[O:3]
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 15077125Methyl 5-(chlorosulfonyl)-1,3-thiazole-4-carboxylate

생성물 1

HCID 15077126Methyl 5-sulfamoyl-1,3-thiazole-4-carboxylate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 28.9 g of methyl 5-(chlorosulfonyl)-4-thiazolecarboxylate in 150 ml tetrahydrofuran was cooled to 0° and 6.6 ml of liquid ammonia was added dropwise at 0°-10°. The suspension was allowed to warm to ambient temperature and stirred 1 hour. The reaction mixture was filtered, the ammonium chloride washed with tetrahydrofuran, and the solvent evaporated from the filtrate. The residual solid was slurried in hexane, collected and dried to give 25.0 g of the title compound, m.p. 138°-140°. IR: 3.01 and 3.1μ (SO2NH2) and 5.8μ (C=O).

후처리

  1. filtrationThe reaction mixture was filtered
  2. washthe ammonium chloride washed with tetrahydrofuran
  3. customthe solvent evaporated from the filtrate
  4. customcollected
  5. customdried

출처 및 근거

ORD 기록
ord-288027ee87514240a048d654d6e10fec
출처 데이터셋
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04919706

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