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1-benzyl-1H-pyrazol-4-amine → 5-(1-Benzyl-1H-pyrazol-4-ylamino)-2-(4-methyl-imidazol-1-yl)-benzonitrile

HRID 2063658
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인쇄 미리보기

반응식

HRID 2063658 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]([N:10]2[CH:14]=[C:13]([CH3:15])[N:12]=[CH:11]2)=[C:6]([CH:9]=1)[C:7]#[N:8].[CH2:16]([N:23]1[CH:27]=[C:26]([NH2:28])[CH:25]=[N:24]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH2:16]([N:23]1[CH:27]=[C:26]([NH:28][C:2]2[CH:3]=[CH:4][C:5]([N:10]3[CH:14]=[C:13]([CH3:15])[N:12]=[CH:11]3)=[C:6]([CH:9]=2)[C:7]#[N:8])[CH:25]=[N:24]1)[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 2066941-benzyl-1H-pyrazol-4-amineHCID 669615175-bromo-2-(4-methyl-1H-imidazol-1-yl)benzonitrile

생성물 1

HCID 593240585-(1-Benzyl-1H-pyrazol-4-ylamino)-2-(4-methyl-imidazol-1-yl)-benzonitrile

실험 절차

Prepared in analogy to example 1b) starting with 5-bromo-2-(4-methyl-imidazol-1-yl)-benzonitrile and 1-benzyl-1H-pyrazol-4-ylamine. The title compound was obtained as a yellow oil (Yield=40%). MS ISP (m/e): 355.2 (100) [(M+H)+].

후처리

  1. customPrepared in analogy to example 1b)

출처 및 근거

ORD 기록
ord-71a524a2503a43d5a4903da60fd7e388
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08288403B2

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