2-Amino-6-methylpyridine → (5-Methyl-2-phenanthren-9-yl-imidazo[1,2-a]pyridin-3-yl)-(1,1,3,3-tetramethylbutyl)-amine

HRID 22813

반응식

HRID 22813 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=1.[CH3:9][C:10]([N+:17]#[C-:18])([CH3:16])[CH2:11][C:12]([CH3:15])([CH3:14])[CH3:13].[CH:19]1[C:32]2[CH:31]=[C:30]([CH:33]=O)[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[C:23]=2[CH:22]=[CH:21][CH:20]=1>Cl(O)(=O)(=O)=O>[CH3:8][C:4]1[N:3]2[C:18]([NH:17][C:10]([CH3:16])([CH3:9])[CH2:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[C:33]([C:30]3[C:29]4[C:24]([C:23]5[CH:22]=[CH:21][CH:20]=[CH:19][C:32]=5[CH:31]=3)=[CH:25][CH:26]=[CH:27][CH:28]=4)[N:1]=[C:2]2[CH:7]=[CH:6][CH:5]=1

참가 물질

5

실험 절차

Compound (36) was prepared according to the general synthesis instructions from 1.0 ml of 2-amino-6-methylpyridine solution (0.1 M, DCM), 0.575 ml of 1,1,3,3-tetramethylbutyl isocyanide solution (0.2 M, DCM), 0.500 ml of phenanthrene-9-carbaldehyde solution (0.3 M, DCM), and 10 μl of perchloric acid (w=20%).

출처 및 근거

ORD 기록
ord-dfda71c95a32446db74fee15f2c8a064
출처 데이터셋
uspto-grants-2005_02
특허 번호
US06849642B2

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