HRID11279

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID1049

Pyridine

C5H5N

HCID3604458

(3,4-Dimethoxyphenyl)acetyl chloride

C10H11ClO3

结构：CCOc1ccc(N)cc1-c1nn2c(C3CCCC3)nc(C)c2c(=O)[nH]1

HCID135604941

未命名化合物

PRODUCTS

生成物

结构：CCOc1ccc(NC(=O)Cc2ccc(OC)c(OC)c2)cc1-c1nn2c(C3CCCC3)nc(C)c2c(=O)[nH]1

HCID135604951

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID8028

Tetrahydrofuran

C4H8O

PROCEDURE

实验过程

Analogously to the preparation of example 46, 100 mg (0.283 mmol) of the compound from example 42A are reacted with 182 mg (0.849 mmol) of 3,4-dimethoxyphenylacetyl chloride and 0.23 ml (2.84 mmol) of pyridine in 6 ml of tetrahydrofuran.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0d637d190c36455992e0de19f9749e14
来源数据集: uspto-grants-2006_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07098207B2
来源说明: uspto-grants-2006_08

反应 SMILES

[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([O:24][CH2:25][CH3:26])=[C:6]([C:8]2[NH:13][C:12](=[O:14])[C:11]3=[C:15]([CH3:23])[N:16]=[C:17]([CH:18]4[CH2:22][CH2:21][CH2:20][CH2:19]4)[N:10]3[N:9]=2)[CH:7]=1.[CH3:27][O:28][C:29]1[CH:30]=[C:31]([CH2:37][C:38](Cl)=[O:39])[CH:32]=[CH:33][C:34]=1[O:35][CH3:36].N1C=CC=CC=1>O1CCCC1>[CH3:27][O:28][C:29]1[CH:30]=[C:31]([CH2:37][C:38]([NH:1][C:2]2[CH:3]=[CH:4][C:5]([O:24][CH2:25][CH3:26])=[C:6]([C:8]3[NH:13][C:12](=[O:14])[C:11]4=[C:15]([CH3:23])[N:16]=[C:17]([CH:18]5[CH2:22][CH2:21][CH2:20][CH2:19]5)[N:10]4[N:9]=3)[CH:7]=2)=[O:39])[CH:32]=[CH:33][C:34]=1[O:35][CH3:36]