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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethylamine → 5-Chloro-2-morpholinophenylguanidine

HRID 1588688
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HRID 1588688 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:11]2[CH2:16][CH2:15][O:14][CH2:13][CH2:12]2)=[C:6]([NH:8][C:9]#[N:10])[CH:7]=1.C[NH:18]C>C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:11]2[CH2:16][CH2:15][O:14][CH2:13][CH2:12]2)=[C:6]([NH:8][C:9]([NH2:18])=[NH:10])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 674DimethylamineHCID 18952323N-(5-chloro-2-morpholinophenyl)cyanamide

생성물 1

HCID 1785125605-Chloro-2-morpholinophenylguanidine

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

In a similar manner to that described in Example 272, N-(5-chloro-2-morpholinophenyl)cyanamide (2.3 g) in ethanol (10 ml) and a 33% ethanolic solution of dimethylamine (6 ml) were heated under reflux for 4 hours to give 1,1-dimethyl-2-(5-chloro-2-morpholinophenylguanidine (m.p. 135°-138° C.) which was recrystallised from hexane and then was converted into its monofumarate salt (m.p. 223°-225° C.) which was recrystallised from methanol.

후처리

  1. temperatureunder reflux for 4 hours

출처 및 근거

ORD 기록
ord-f4ac72f7bee24272a68ed04e653cac00
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05223498

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