HRID1493531

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID13140

Acrylyl chloride

C3H3ClO

结构：CCCCCCCC(ON1C(C)(C)CC(O)CC1(C)C)ON1C(C)(C)CC(O)CC1(C)C

HCID23372110

未命名化合物

PRODUCTS

生成物

结构：C=CC(=O)OC1CC(C)(C)N(OC(CCCCCCC)ON2C(C)(C)CC(OC(=O)C=C)CC2(C)C)C(C)(C)C1

HCID19778495

未命名化合物

PROCEDURE

实验过程

The title compound is prepared by the reaction of the compound prepared in Example 4 with acryloyl chloride.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-3b46a22ea0724b21a0a554676a2243ac
来源数据集: uspto-grants-1991_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05021577
来源说明: uspto-grants-1991_06

反应 SMILES

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