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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 5-(Ethanesulfonyl)-1,3-benzothiazol-2-amine

HRID 1383063
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HRID 1383063 반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH2:11][CH3:12])(=[O:10])=[O:9])=[CH:4][C:3]=1[N+:13]([O-])=O.[NH2:16][C:17](N)=[S:18].O>S1(CCCC1)(=O)=O>[NH2:16][C:17]1[S:18][C:2]2[CH:7]=[CH:6][C:5]([S:8]([CH2:11][CH3:12])(=[O:10])=[O:9])=[CH:4][C:3]=2[N:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 15158591-Chloro-4-(ethylsulfonyl)-2-nitrobenzeneHCID 2723790Thiourea

생성물 1

HCID 212739825-(Ethanesulfonyl)-1,3-benzothiazol-2-amine수율 85.3%

시약·촉매·용매 1

HCID 31347Sulfolane용매

반응 조건

온도
120 °C

실험 절차

A suspension of 12.8 g of ethyl 4-chloro-3-nitrophenyl sulphone and 15.2 g of thiourea in 50 ml of sulpholane is heated to 120° C. and this temperature is maintained for 1.5 hours. The mixture is discharged into 600 ml of water, and the solid is filtered off with suction and washed with water. 10.6 g of colourless 2-amino-5-ethanesulphonylbenzothiazole are obtained.

후처리

  1. temperaturethis temperature is maintained for 1.5 hours
  2. filtrationthe solid is filtered off with suction
  3. washwashed with water

출처 및 근거

ORD 기록
ord-e308b529ecba4678aba7c09a10c6a3eb
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04808723

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