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Fumaric Acid → 2-[3-(2-Cyanopyrrol-1-yl)benzoyl]guanidine fumarate

HRID 399872
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HRID 399872 반응식
[C:1]([OH:8])(=[O:7])/[CH:2]=[CH:3]/[C:4]([OH:6])=[O:5].[C:9]([C:11]1[N:12]([C:16]2[CH:17]=[C:18]([CH:25]=[CH:26][CH:27]=2)[C:19]([N:21]=[C:22]([NH2:24])[NH2:23])=[O:20])[CH:13]=[CH:14][CH:15]=1)#[N:10]>CO>[C:1]([OH:8])(=[O:7])/[CH:2]=[CH:3]/[C:4]([OH:6])=[O:5].[C:9]([C:11]1[N:12]([C:16]2[CH:17]=[C:18]([CH:25]=[CH:26][CH:27]=2)[C:19]([N:21]=[C:22]([NH2:23])[NH2:24])=[O:20])[CH:13]=[CH:14][CH:15]=1)#[N:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 444972Fumaric AcidHCID 189451892-[3-(2-Cyanopyrrol-1-yl)benzoyl]guanidine

생성물 1

HCID 189452202-[3-(2-Cyanopyrrol-1-yl)benzoyl]guanidine fumarate수율 70.6%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

A solution of fumaric acid (0.46 g) in methanol (10 ml) was added to a solution of 2-[3-(2-cyanopyrrol-1-yl)benzoyl]guanidine (1.0 g) in methanol (10 ml) and the whole was stirred for 1 hour at ambient temperature. The isolated precipitate was collected by filtration and the precipitate was recrystallized from methanol-water to give 2-[3-(2-cyanopyrrol-1-yl)benzoyl]guanidine fumarate (1.03 g).

후처리

  1. filtrationThe isolated precipitate was collected by filtration
  2. customthe precipitate was recrystallized from methanol-water

출처 및 근거

ORD 기록
ord-98a8ec2d00e0446191f19efab8e09b1e
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05824691

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