HRID1696991

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID585835

2-(1-Isopropyl-1H-imidazol-4-yl)ethanamine

C8H15N3

结构：O[C@@H]1C=C[C@H](n2cnc3c(Cl)nc(Cl)nc32)C1

HCID10378467

未命名化合物

结构：CCC(=O)N[C@H]1C[C@@H](n2cnc3c(NCC(c4ccccc4)c4ccccc4)nc(Cl)nc32)[C@H](O)[C@@H]1O

HCID86622630

未命名化合物

PRODUCTS

生成物

结构：CCC(=O)N[C@H]1C[C@@H](n2cnc3c(NCC(c4ccccc4)c4ccccc4)nc(NCCc4cn(C(C)C)cn4)nc32)[C@H](O)[C@@H]1O

HCID67019296

未命名化合物

PROCEDURE

实验过程

This compound is prepared from N-{(1S,2R,3S,4R)-4-[2-chloro-6-(2,2-diphenyl-ethylamino)-purin-9-yl]-2,3-dihydroxy-cyclopentyl}-propionamide (compound of Example 4) and 2-(1-isopropyl-1H-imidazol-4-yl)-ethylamine using a procedure analogous to that of Example 9 for the desired salt. MS (ES+) m/e 638 (MH+).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-c82acaba57d54655b6917cb9dd3c73ee
来源数据集: uspto-grants-2012_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08163754B2
来源说明: uspto-grants-2012_04

反应 SMILES

Cl[C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[C@@H:11]2[CH2:15][C@H:14]([NH:16][C:17](=[O:20])[CH2:18][CH3:19])[C@@H:13]([OH:21])[C@H:12]2[OH:22])=[C:4]([NH:23][CH2:24][CH:25]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[N:3]=1.ClC1N=C2C(N=CN2[C@@H]2C[C@H](O)C=C2)=C(Cl)N=1.[CH:55]([N:58]1[CH:62]=[C:61]([CH2:63][CH2:64][NH2:65])[N:60]=[CH:59]1)([CH3:57])[CH3:56]>>[C:26]1([CH:25]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH2:24][NH:23][C:4]2[N:3]=[C:2]([NH:65][CH2:64][CH2:63][C:61]3[N:60]=[CH:59][N:58]([CH:55]([CH3:57])[CH3:56])[CH:62]=3)[N:10]=[C:9]3[C:5]=2[N:6]=[CH:7][N:8]3[C@@H:11]2[CH2:15][C@H:14]([NH:16][C:17](=[O:20])[CH2:18][CH3:19])[C@@H:13]([OH:21])[C@H:12]2[OH:22])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1