HRID1643397

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID170103

8-Quinolinecarboxaldehyde

C10H7NO

结构：Ic1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1

HCID618252

4-iodo-1-tritylimidazole

C22H17IN2

HCID59749553

未命名化合物

结构：Cc1ncn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c1C(O)c1cccc2cccnc12

HCID66755693

未命名化合物

PRODUCTS

生成物

结构：Cc1c(C(=O)c2cn(C(c3ccccc3)(c3ccccc3)c3ccccc3)cn2)ccc2cccnc12

HCID59749533

未命名化合物

PROCEDURE

实验过程

(8-Methylquinolin-7-yl)(1-trityl-1H-imidazol-4-yl)methanone (21) was synthesized from (20) and 4-iodo-1-trityl-1H-imidazole via the procedure used in the preparation of (4) from (3) above.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-5bf0a6be995d44e19c3300cf564637d5
来源数据集: uspto-grants-2012_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08119807B2
来源说明: uspto-grants-2012_02

反应 SMILES

CON(C)[C:4]([C:6]1[C:15]([CH3:16])=[C:14]2[C:9]([CH:10]=[CH:11][CH:12]=[N:13]2)=[CH:8][CH:7]=1)=[O:5].I[C:19]1[N:20]=[CH:21][N:22]([C:24]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH:23]=1.CC1N=CN(C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)C=1C(C1C=CC=C2C=1N=CC=C2)O.N1C2C(=CC=CC=2C=O)C=CC=1>>[CH3:16][C:15]1[C:6]([C:4]([C:19]2[N:20]=[CH:21][N:22]([C:24]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)([C:37]3[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=3)[C:31]3[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=3)[CH:23]=2)=[O:5])=[CH:7][CH:8]=[C:9]2[C:14]=1[N:13]=[CH:12][CH:11]=[CH:10]2