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Toluene → N'-(2-chlorocyclohexyl)-urea

HRID 1580322
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인쇄 미리보기

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HRID 1580322 반응식
C1(S([NH:10][C:11](N)=[O:12])(=O)=O)C=CC=CC=1.C1(C)C=CC=CC=1.[Cl:21][CH:22]1[CH2:27][CH2:26][CH2:25][CH2:24][CH:23]1[NH2:28]>C(O)(=O)C>[Cl:21][CH:22]1[CH2:27][CH2:26][CH2:25][CH2:24][CH:23]1[NH:28][C:11](=[O:12])[NH2:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1140TolueneHCID 118791N-(aminocarbonyl)benzenesulphonamideHCID 4188002-Chlorocyclohexan-1-amine

생성물 1

HCID 85911145N'-(2-chlorocyclohexyl)-urea

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 10.3 g of of N-[4-<2-methoxy-5-chlorobenzamido>-ethyl)-benzenesulfonyl]-ethyl)-benzenesulfonyl-urea (melting point 171° -173°C), 300 ml of toluene, 30 ml of glycolmonomethyl-ether, 1.65 g of glacial acetic acid and 3.3 g of 2-chloro-cyclohexylamine are heated under reflux for 5 hours. Then the whole is concentrated in vacuo and the residue is treated with alcohol. The N-[4-(β<2-methoxy-5-chlorobenzamido> -ethyl)-benzenesulfonyl]-N'-(2-chlorocyclohexyl)-urea obtained as crude product melts at 194° -195°C after recrystallization from methanol/dimethylformamide.

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후처리

  1. temperatureare heated
  2. temperatureunder reflux for 5 hours
  3. concentrationThen the whole is concentrated in vacuo
  4. additionthe residue is treated with alcohol

출처 및 근거

ORD 기록
ord-2336f2a4baa044938270d14e125c5e92
출처 데이터셋
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03932503

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