HRID2228943

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID76824

Carbonazidic acid, diphenylmethyl ester

C14H11N3O2

HCID22180413

未命名化合物

PRODUCTS

生成物

结构：O=C(OC(c1ccccc1)c1ccccc1)N1CCN(c2ccc3c(c2)C(=O)N(C2CCCCC2)C3)CC1

HCID12043721

未命名化合物

PROCEDURE

实验过程

In the same manner as in Example 28, the title compound was prepared from the compound obtained in step (e) of Example 1 and benzhydryloxycarbonyl azide.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b062de23bcd54d44b5845821f92d2ba6
来源数据集: uspto-grants-2002_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06417362B1
来源说明: uspto-grants-2002_07

反应 SMILES

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