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Ammonia → 4-(2,4-Dichloro-5-sulfamoylphenyl)-3-methyl-2-methylimino-1,3-thiazolidine-4-ol

HRID 460834
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HRID 460834 반응식
Br.[Cl:2][C:3]1[CH:8]=[C:7]([Cl:9])[C:6]([S:10](Cl)(=[O:12])=[O:11])=[CH:5][C:4]=1[C:14]1([OH:22])[CH2:18][S:17][C:16](=[N:19][CH3:20])[N:15]1[CH3:21].[NH3:23]>CO>[Cl:2][C:3]1[CH:8]=[C:7]([Cl:9])[C:6]([S:10](=[O:12])(=[O:11])[NH2:23])=[CH:5][C:4]=1[C:14]1([OH:22])[CH2:18][S:17][C:16](=[N:19][CH3:20])[N:15]1[CH3:21]
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 213947574-(2,4-Dichlor-5-chlorosulfonylphenyl)-3-methyl-2-methylimino-1,3-thiazolidine-4-ol-hydrobromide

생성물 1

HCID 213947694-(2,4-Dichloro-5-sulfamoylphenyl)-3-methyl-2-methylimino-1,3-thiazolidine-4-ol

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

4.4 g of 4-(2,4-dichlor-5-chlorosulfonylphenyl)-3-methyl-2-methylimino-1,3-thiazolidine-4-ol-hydrobromide were introduced, while stirring, into a solution of 10 g of gaseous ammonia in 70 ml of methanol. After having allowed the whole to stand overnight at room temperature, the solution was concentrated to about 30 ml of its volume under reduced pressure and the 4-(2,4-dichloro-5-sulfamoylphenyl)-3-methyl-2-methylimino-1,3-thiazolidine-4-ol was precipitated with 100 ml of water. M.p. 186°-189° C (decomposition ).

후처리

  1. concentrationthe solution was concentrated to about 30 ml of its volume under reduced pressure
  2. customthe 4-(2,4-dichloro-5-sulfamoylphenyl)-3-methyl-2-methylimino-1,3-thiazolidine-4-ol was precipitated with 100 ml of water

출처 및 근거

ORD 기록
ord-616116e7316d4819bb38c8d4348c99b8
출처 데이터셋
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04061647

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