HRID627136

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：C=CCON([C@@H]1C=C(C(C)C)[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1)S(=O)(=O)c1ccccc1[N+](=O)[O-]

HCID89852135

未命名化合物

2 次

结构：C=CCON([C@@H]1C=C(C)[C@@H](C(N)=O)N(C(=O)OC(C)(C)C)C1)S(=O)(=O)c1ccccc1[N+](=O)[O-]

HCID89852450

未命名化合物

PRODUCTS

生成物

结构：C=CCON([C@@H]1C=C(C(C)C)[C@@H](C(N)=O)N(C(=O)OC(C)(C)C)C1)S(=O)(=O)c1ccccc1[N+](=O)[O-]

HCID89852417

未命名化合物

收率 43.7%

PROCEDURE

实验过程

(2S,5R)-tert-butyl 5-(N-(allyloxy)-2-nitrophenylsulfonamido)-2-carbamoyl-3-isopropyl-5,6-dihydropyridine-1(2H)-carboxylate (0.260 g, 43.7%) was prepared a similar manner as described in Intermediate 83 as a pale yellow oil, using (2S,5R)-5-(N-(allyloxy)-2-nitrophenylsulfonamido)-1-(tert-butoxycarbonyl)-3-isopropyl-1,2,5,6-tetrahydropyridine-2-carboxylic acid (Intermediate 93, 0.595 g, 1.13 mmol) as a starting material.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-fae6d740e3394e9c926503d0615a2fbd
来源数据集: uspto-grants-2016_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09309245B2
来源说明: uspto-grants-2016_04

反应 SMILES

C(O[N:5]([C@H]1CN(C(OC(C)(C)C)=O)[C@H](C(=O)N)C(C)=C1)S(C1C=CC=CC=1[N+]([O-])=O)(=O)=O)C=C.[CH2:35]([O:38][N:39]([C@H:52]1[CH2:57][N:56]([C:58]([O:60][C:61]([CH3:64])([CH3:63])[CH3:62])=[O:59])[C@H:55]([C:65]([OH:67])=O)[C:54]([CH:68]([CH3:70])[CH3:69])=[CH:53]1)[S:40]([C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][C:44]=1[N+:49]([O-:51])=[O:50])(=[O:42])=[O:41])[CH:36]=[CH2:37]>>[CH2:35]([O:38][N:39]([C@H:52]1[CH2:57][N:56]([C:58]([O:60][C:61]([CH3:63])([CH3:64])[CH3:62])=[O:59])[C@H:55]([C:65](=[O:67])[NH2:5])[C:54]([CH:68]([CH3:70])[CH3:69])=[CH:53]1)[S:40]([C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][C:44]=1[N+:49]([O-:51])=[O:50])(=[O:41])=[O:42])[CH:36]=[CH2:37]