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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Aminothiazole → 2-Amino-3-methylthiazolium p-toluenesulfonate

HRID 53230
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인쇄 미리보기

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HRID 53230 반응식
[NH2:1][C:2]1[S:3][CH:4]=[CH:5][N:6]=1.[C:7]1([CH3:18])[CH:12]=[CH:11][C:10]([S:13]([O:16]C)(=[O:15])=[O:14])=[CH:9][CH:8]=1>CC(C)=O>[C:7]1([CH3:18])[CH:8]=[CH:9][C:10]([S:13]([O-:16])(=[O:14])=[O:15])=[CH:11][CH:12]=1.[NH2:1][C:2]1[S:3][CH:4]=[CH:5][N+:6]=1[CH3:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21552-AminothiazoleHCID 6645Methyl p-toluenesulfonate

생성물 1

HCID 199621872-Amino-3-methylthiazolium p-toluenesulfonate

시약·촉매·용매 1

HCID 180Acetone용매

반응 조건

온도
60 °C

실험 절차

In a 200 ml three-necked flask were placed 2.0 g of 2-aminothiazole and 5.6 g of methyl p-toluenesulfonate, and the mixture was stirred at 120° C. for 4 hours. After the resulting mixture was cooled to 60° C., 100 ml of acetone was added and the mixture was stirred for 1 hour. The precipitates were filtered under reduced pressure, washed with acetone, and dried at room temperature under reduced pressure.

후처리

  1. customIn a 200 ml three-necked flask were placed
  2. filtrationThe precipitates were filtered under reduced pressure
  3. washwashed with acetone
  4. customdried at room temperature under reduced pressure

출처 및 근거

ORD 기록
ord-395da0d658534a0ebfa6c8c8e18e359e
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05618831

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