HRID1691484

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：Cc1cc(C(C)(O)c2ccc3c(c2)N(S(=O)(=O)c2ccc(OC(F)(F)F)cc2)Cc2ccc(C(F)(F)F)nc2N3)n[nH]1

HCID59618628

未命名化合物

结构：Cc1cc(C(=O)c2ccc3c(c2)N(S(=O)(=O)c2ccc(OC(F)(F)F)cc2)Cc2ccc(C(F)(F)F)nc2N3)n[nH]1

HCID59618680

未命名化合物

PRODUCTS

生成物

HCID59618750

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from (5-methyl-1H-pyrazol-3-yl)[6-{[4-(trifluoromethoxy)phenyl]sulfonyl}-2-(trifluoromethyl)-6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-8-yl]methanone (the product of Example 527, Step B) using the procedure described in Example 511; Mass Spectrum: m/e=600 (M+1).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-c31da3c13abf426eb61d70bd6cffa2b6
来源数据集: uspto-grants-2012_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08153626B2
来源说明: uspto-grants-2012_04

反应 SMILES

[CH3:1][C:2]1[NH:6][N:5]=[C:4]([C:7]([C:9]2[CH:10]=[CH:11][C:12]3[NH:18][C:17]4[N:19]=[C:20]([C:23]([F:26])([F:25])[F:24])[CH:21]=[CH:22][C:16]=4[CH2:15][N:14]([S:27]([C:30]4[CH:35]=[CH:34][C:33]([O:36][C:37]([F:40])([F:39])[F:38])=[CH:32][CH:31]=4)(=[O:29])=[O:28])[C:13]=3[CH:41]=2)=[O:8])[CH:3]=1.CC1NN=C(C(C2C=CC3NC4N=C(C(F)(F)F)C=CC=4CN(S(C4C=CC(OC(F)(F)F)=CC=4)(=O)=O)C=3C=2)(O)C)C=1>>[CH3:1][C:2]1[NH:6][N:5]=[C:4]([CH:7]([C:9]2[CH:10]=[CH:11][C:12]3[NH:18][C:17]4[N:19]=[C:20]([C:23]([F:24])([F:25])[F:26])[CH:21]=[CH:22][C:16]=4[CH2:15][N:14]([S:27]([C:30]4[CH:35]=[CH:34][C:33]([O:36][C:37]([F:39])([F:40])[F:38])=[CH:32][CH:31]=4)(=[O:29])=[O:28])[C:13]=3[CH:41]=2)[OH:8])[CH:3]=1