HRID2271688

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2734650

2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

C13H19BO4

结构：CC(C)(C)OC(=O)N[C@H]1CC[C@H](Nc2c(C(=O)C3CC3)cnc3ccc(Br)cc23)CC1

HCID178454009

未命名化合物

PRODUCTS

生成物

结构：COc1cc(-c2ccc3ncc(C(=O)C4CC4)c(N[C@H]4CC[C@H](NC(=O)OC(C)(C)C)CC4)c3c2)ccc1O

HCID178487419

未命名化合物

收率 85%

PROCEDURE

实验过程

Following general procedure D, tert-butyl trans-4-[6-bromo-3-(cyclopropanecarbonyl)quinolin-4-ylamino]cyclohexylcarbamate (49 mg, 0.100 mmol) was reacted with 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (50 mg, 0.200 mmol) to afford the desired product (45 mg, 85%) as an off-white solid: ESI MS m/z 532 [C31H37N3O5+H]+.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0cb10b8a88364e659e3d81eeb7ddea73
来源数据集: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09120749B2
来源说明: uspto-grants-2015_09

反应 SMILES

Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6]([C:12]([CH:14]1[CH2:16][CH2:15]1)=[O:13])=[C:5]2[NH:17][C@H:18]1[CH2:23][CH2:22][C@H:21]([NH:24][C:25](=[O:31])[O:26][C:27]([CH3:30])([CH3:29])[CH3:28])[CH2:20][CH2:19]1.[CH3:32][O:33][C:34]1[CH:39]=[C:38](B2OC(C)(C)C(C)(C)O2)[CH:37]=[CH:36][C:35]=1[OH:49]>>[CH:14]1([C:12]([C:6]2[CH:7]=[N:8][C:9]3[C:4]([C:5]=2[NH:17][C@H:18]2[CH2:23][CH2:22][C@H:21]([NH:24][C:25](=[O:31])[O:26][C:27]([CH3:29])([CH3:30])[CH3:28])[CH2:20][CH2:19]2)=[CH:3][C:2]([C:38]2[CH:37]=[CH:36][C:35]([OH:49])=[C:34]([O:33][CH3:32])[CH:39]=2)=[CH:11][CH:10]=3)=[O:13])[CH2:16][CH2:15]1