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Pyridine → Ethyl 2-methanesulfonamidothiazol-5-ylacetate

HRID 127104
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HRID 127104 반응식
[NH2:1][C:2]1[S:3][C:4]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:5][N:6]=1.N1C=CC=CC=1.[S:19](Cl)([CH3:22])(=[O:21])=[O:20]>C(Cl)Cl>[CH3:22][S:19]([NH:1][C:2]1[S:3][C:4]([CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:5][N:6]=1)(=[O:21])=[O:20]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 31297Methanesulfonyl chlorideHCID 717815Ethyl 2-(2-amino-1,3-thiazol-5-yl)acetate

생성물 1

HCID 20288652Ethyl 2-methanesulfonamidothiazol-5-ylacetate수율 60.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

To a solution of ethyl 2-aminothiazol-5-ylacetate (32 g.) in methylene chloride (160 ml.) was added pyridine (27.2 g.) under ice-cooling, and to the mixture was dropwise added mesyl chloride (29.6 g.) in methylene chloride (29.6 ml.) over 30 minutes at 8° to 10° C. The mixture was further stirred for 8 hours at room temperature. After the reaction, methylene chloride was distilled off from the reaction mixture, and to the residue were added water (300 ml.) and ethyl acetate (300 ml.). The resulting mixture was adjusted to pH 2 with 10% hydrochloric acid under ice-cooling, and the precipitates were collected by filtration and washed with ethyl acetate. The precipitates were recrystallized from ethanol (600 ml.) to give ethyl 2-methanesulfonamidothiazol-5-ylacetate (27.3 g.), mp 153° to 155° C.

후처리

  1. temperaturecooling
  2. customover 30 minutes
  3. customat 8° to 10° C
  4. distillationwas distilled off from the reaction mixture
  5. additionto the residue were added water (300 ml.) and ethyl acetate (300 ml.)
  6. temperaturecooling
  7. filtrationthe precipitates were collected by filtration
  8. washwashed with ethyl acetate
  9. customThe precipitates were recrystallized from ethanol (600 ml.)

출처 및 근거

ORD 기록
ord-3dad1036b9dd452d961c4d42bc138ca6
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04254260

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