HRID1161576

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6454398

2-Pyridone hydrazone dihydrochloride

C5H9Cl2N3

结构：CC(=O)O.COc1cc([C@H](Nc2ccc(C(=N)N)cc2)c2nn(-c3ncccn3)c(=O)[nH]2)cc2c1OCOC2

HCID136366222

未命名化合物

PRODUCTS

生成物

结构：CC(=O)O.COc1cc([C@H](Nc2ccc(C(=N)N)cc2)c2nn(-c3ccccn3)c(=O)[nH]2)cc2c1OCOC2

HCID136389289

未命名化合物

PROCEDURE

实验过程

The same procedure was carried out as in Examples (21i) to (21k), except that 2-hydrazinopyridine dihydrochloride was used instead of 2-hydrazinopyrimidine in Example (21i), to give the first eluting enantiomer of the title compound.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b341856b902f401f98b626e3a2531f5f
来源数据集: uspto-grants-2010_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07816522B2
来源说明: uspto-grants-2010_10

反应 SMILES

[C:1]([OH:4])(=[O:3])[CH3:2].[CH3:5][O:6][C:7]1[C:16]2[O:15][CH2:14][O:13][CH2:12][C:11]=2[CH:10]=[C:9]([C@H:17]([NH:30][C:31]2[CH:39]=[CH:38][C:34]([C:35]([NH2:37])=[NH:36])=[CH:33][CH:32]=2)[C:18]2[NH:22][C:21](=[O:23])[N:20]([C:24]3N=[CH:28][CH:27]=[CH:26][N:25]=3)[N:19]=2)[CH:8]=1.Cl.Cl.N([C:44]1C=CC=CN=1)N>>[C:1]([OH:4])(=[O:3])[CH3:2].[CH3:5][O:6][C:7]1[C:16]2[O:15][CH2:14][O:13][CH2:12][C:11]=2[CH:10]=[C:9]([C@H:17]([NH:30][C:31]2[CH:39]=[CH:38][C:34]([C:35]([NH2:37])=[NH:36])=[CH:33][CH:32]=2)[C:18]2[NH:22][C:21](=[O:23])[N:20]([C:24]3[CH:44]=[CH:28][CH:27]=[CH:26][N:25]=3)[N:19]=2)[CH:8]=1