HRID1260764

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7127818

3-(5-methyl-1,2,4-oxadiazol-3-yl)benzoic acid

C10H8N2O3

结构：Cl.Cl.Cl.N[C@H]1CC[C@H](CCN2CCN(c3nccc4c3OCC4)CC2)CC1

HCID178478590

未命名化合物

2 次

PRODUCTS

生成物

结构：Cc1nc(-c2cccc(C(=O)N[C@H]3CC[C@H](CCN4CCN(c5nccc6c5OCC6)CC4)CC3)c2)no1

HCID178432504

未命名化合物

PROCEDURE

实验过程

The title compound, white solid (120 mg, 93%), MS (ISP) m/z=517.5 [(M+H)+], mp 227.5° C., was prepared in accordance with the general method of example 6 from trans-4-{2-[4-(2,3-dihydro-furo[2,3-c]pyridin-7-yl)-piperazin-1-yl]-ethyl}-cyclohexylamine trihydrochloride (intermediate B) (110 mg, 0.25 mmol) and 3-(5-methyl-[1,2,4]oxadiazol-3-yl)-benzoic acid.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-a70bf6a17f724c5ea53f9ec777941352
来源数据集: uspto-grants-2013_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08470828B2
来源说明: uspto-grants-2013_06

反应 SMILES

Cl.Cl.Cl.[O:4]1[C:8]2=[C:9]([N:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][C@H:21]4[CH2:26][CH2:25][C@H:24]([NH2:27])[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[N:10]=[CH:11][CH:12]=[C:7]2[CH2:6][CH2:5]1.[CH3:28][C:29]1[O:33][N:32]=[C:31]([C:34]2[CH:35]=[C:36]([CH:40]=[CH:41][CH:42]=2)[C:37](O)=[O:38])[N:30]=1>>[O:4]1[C:8]2=[C:9]([N:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][C@H:21]4[CH2:26][CH2:25][C@H:24]([NH:27][C:37](=[O:38])[C:36]5[CH:40]=[CH:41][CH:42]=[C:34]([C:31]6[N:30]=[C:29]([CH3:28])[O:33][N:32]=6)[CH:35]=5)[CH2:23][CH2:22]4)[CH2:15][CH2:14]3)[N:10]=[CH:11][CH:12]=[C:7]2[CH2:6][CH2:5]1