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Ethyl p-methylbenzenesulfonate → 2-Amino-3-ethyl-6-methoxybenzothiazolium p-toluenesulfonate

HRID 53232
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인쇄 미리보기

반응식

HRID 53232 반응식
[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:5]=2[N:6]=1.[C:13]1([CH3:25])[CH:18]=[CH:17][C:16]([S:19]([O:22]CC)(=[O:21])=[O:20])=[CH:15][CH:14]=1>CC(C)=O>[C:13]1([CH3:25])[CH:14]=[CH:15][C:16]([S:19]([O-:22])(=[O:20])=[O:21])=[CH:17][CH:18]=1.[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:5]=2[N+:6]=1[CH2:13][CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6638Ethyl p-methylbenzenesulfonateHCID 156302-Amino-6-methoxybenzothiazole

생성물 1

HCID 199622022-Amino-3-ethyl-6-methoxybenzothiazolium p-toluenesulfonate

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

In a 200 ml three-necked flask were placed 3.6 g of 2-amino-6-methoxybenzothiazole and 6.0 g of ethyl p-toluenesulfonate, and the mixture was stirred at 120° C. for 3 hours. To the resulting mixture was added acetone and the mixture was stirred at room temperature for 1 hour. The crystals were filtered under reduced pressure and washed with acetone to give the desired compound.

후처리

  1. customIn a 200 ml three-necked flask were placed
  2. filtrationThe crystals were filtered under reduced pressure
  3. washwashed with acetone

출처 및 근거

ORD 기록
ord-4114cf9256a548029a1682dd29f9b3a3
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05618831

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