HRID521855

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：Cn1ncc([N+](=O)[O-])c1C1(F)CCC(O)C(NC(=O)OC(C)(C)C)CC1

HCID86713008

未命名化合物

结构：Cn1ncc(NC(=O)c2nc(-c3c(F)cccc3F)sc2NC(=O)OC(C)(C)C)c1Cl

HCID86713771

未命名化合物

PRODUCTS

生成物

结构：Cn1ncc(NC(=O)c2nc(-c3ccccc3F)sc2NC(=O)OC(C)(C)C)c1C12CCC(NC(=O)OC(C)(C)C)C(CC1)O2

HCID86713802

未命名化合物

PROCEDURE

实验过程

Following the procedure for Intermediate 1 starting from tert-butyl N-(5-fluoro-2-hydroxy-5-(2-methyl-4-nitro-pyrazol-3-yl)cycloheptyl)carbamate gave tert-butyl N-(5-[4-((5-(tert-butoxycarbonylamino)-2-(2-fluorophenyl)thiazole-4-carbonyl)amino)-2-methyl-pyrazol-3-yl]-8-oxabicyclo[3.2.1]octan-2-yl]carbamate as a pale pink solid (310 mg, 31% over two steps). 1H NMR (400 MHz, CDCl3) δ 10.50 (br s, 1H), 10.48 (s, 1H), 8.39-8.29 (m, 2H), 7.60-7.51 (m, 1H), 7.38-7.31 (m, 1H), 7.18 (dd, J=11.4, 8.3 Hz, 1H), 4.86 (br s, 1H), 4.36 (br s, 1H), 4.07 (br s, 1H), 3.86 (s, 3H), 2.43-2.35 (m, 1H), 2.22-1.92 (m, 7H), 1.55 (s, 9H), 1.50 (s, 9H).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0269d6239f95482291fa34b398bfe901
来源数据集: uspto-grants-2016_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09328106B2
来源说明: uspto-grants-2016_05

反应 SMILES

Cl[C:2]1[N:6]([CH3:7])[N:5]=[CH:4][C:3]=1[NH:8][C:9]([C:11]1[N:12]=[C:13]([C:24]2[C:29](F)=[CH:28][CH:27]=[CH:26][C:25]=2[F:31])[S:14][C:15]=1[NH:16][C:17](=[O:23])[O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:10].F[C:33]1(C2N(C)N=CC=2[N+]([O-])=O)[CH2:39][CH2:38][CH:37]([NH:40][C:41](=[O:47])[O:42][C:43]([CH3:46])([CH3:45])[CH3:44])[CH:36]([OH:48])[CH2:35][CH2:34]1>>[C:19]([O:18][C:17]([NH:16][C:15]1[S:14][C:13]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=2[F:31])=[N:12][C:11]=1[C:9]([NH:8][C:3]1[CH:4]=[N:5][N:6]([CH3:7])[C:2]=1[C:33]12[O:48][CH:36]([CH2:35][CH2:34]1)[CH:37]([NH:40][C:41](=[O:47])[O:42][C:43]([CH3:46])([CH3:45])[CH3:44])[CH2:38][CH2:39]2)=[O:10])=[O:23])([CH3:22])([CH3:21])[CH3:20]