HRID2265512

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID14517153

2-(Chloromethyl)-5-methoxypyridine

C7H8ClNO

结构：CC(C)c1ccc(N(Cc2cn[nH]c2)C(=O)C2CCCc3ccccc32)cn1.Cl

HCID67183012

未命名化合物

PRODUCTS

生成物

结构：COc1ccc(Cn2cc(CN(C(=O)C3CCCc4ccccc43)c3ccc(C(C)C)nc3)cn2)nc1.Cl.Cl

HCID67183093

未命名化合物

收率 73.8%

PROCEDURE

实验过程

By the reaction and treatment in the same manner as in Example 334 using N-(6-isopropylpyridin-3-yl)-N-[(pyrazol-4-yl)methyl]-1,2,3,4-tetrahydronaphthalene-1-carboxamide hydrochloride (0.95 g) and 2-chloromethyl-5-methoxypyridine (0.83 g) as starting materials, N-(6-isopropylpyridin-3-yl)-N-({1-[(5-methoxypyridin-2-yl)methyl]pyrazol-4-yl}methyl)-1,2,3,4-tetrahydronaphthalene-1-carboxamide dihydrochloride (0.97 g) was obtained.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d92a5ea43629443fb8edf0a1c6c90174
来源数据集: uspto-grants-2010_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07855297B2
来源说明: uspto-grants-2010_12

反应 SMILES

[ClH:1].[CH:2]([C:5]1[N:10]=[CH:9][C:8]([N:11]([CH2:24][C:25]2[CH:26]=[N:27][NH:28][CH:29]=2)[C:12]([CH:14]2[C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH2:17][CH2:16][CH2:15]2)=[O:13])=[CH:7][CH:6]=1)([CH3:4])[CH3:3].[Cl:30][CH2:31][C:32]1[CH:37]=[CH:36][C:35]([O:38][CH3:39])=[CH:34][N:33]=1>>[ClH:30].[ClH:1].[CH:2]([C:5]1[N:10]=[CH:9][C:8]([N:11]([CH2:24][C:25]2[CH:26]=[N:27][N:28]([CH2:31][C:32]3[CH:37]=[CH:36][C:35]([O:38][CH3:39])=[CH:34][N:33]=3)[CH:29]=2)[C:12]([CH:14]2[C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH2:17][CH2:16][CH2:15]2)=[O:13])=[CH:7][CH:6]=1)([CH3:4])[CH3:3]