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Hydrochloric Acid → 3-(N-carbethoxymethyl-N-methylsulfamoyl)-thiophene-2-carboxylic acid methyl ester

HRID 28001
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인쇄 미리보기

반응식

HRID 28001 반응식
[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[CH:8][C:9]=1[S:10](Cl)(=[O:12])=[O:11])=[O:4].[CH2:14]([O:16][C:17](=[O:21])[CH2:18][NH:19][CH3:20])[CH3:15].O.Cl>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[CH:8][C:9]=1[S:10](=[O:12])(=[O:11])[N:19]([CH2:18][C:17]([O:16][CH2:14][CH3:15])=[O:21])[CH3:20])=[O:4]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 95849Glycine, N-methyl-, ethyl esterHCID 27367332-Thiophenecarboxylic acid, 3-(chlorosulfonyl)-, methyl ester

생성물 1

HCID 28087943-(N-carbethoxymethyl-N-methylsulfamoyl)-thiophene-2-carboxylic acid methyl ester

시약·촉매·용매 1

HCID 6212
Chloroform
용매

실험 절차

20 G. of 3-chlorosulfonylthiophene-2-carboxylic acid methyl ester are dissolved in absolute chloroform, whereupon 21 g. of sarcosine ethyl ester are added dropwise during 10 minutes. In so doing, the mixture warms up to 50° C. After 20 minutes, the mixture is cooled, shaken once each time with water, 0.5 -N hydrochloric acid and a sodium bicarbonate solution, dried and evaporated. The remaining oil is brought to crystallization with ethanol. There is obtained 3-(N-carbethoxymethyl-N-methyl-sulfamoyl)-thiophene-2-carboxylic acid methyl ester of melting point 84°-85° C.

후처리

  1. customwarms up to 50° C
  2. temperaturethe mixture is cooled
  3. dry with materiala sodium bicarbonate solution, dried
  4. customevaporated
  5. customThe remaining oil is brought to crystallization with ethanol

출처 및 근거

ORD 기록
ord-2225110906404fa992f1514306ee3eba
출처 데이터셋
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04224445

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