HRID2230278

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7510

Nicotinyl alcohol

C6H7NO

结构：CC(C)(C)OC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)OCC1c2ccccc2-c2ccccc21

HCID15295906

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)OC(=O)[C@H](Cc1ccc(OCc2cccnc2)cc1)NC(=O)OCC1c2ccccc2-c2ccccc21

HCID70060206

未命名化合物

PROCEDURE

实验过程

In a manner similar to that described in Example H, the product from Example G ((S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxyphenyl)-propionic acid tert-butyl ester) (4.39 g, 9.50 mmol) and 3-pyridylcarbinol (0.92 mL, 9.50 mmol) were converted to the title compound.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-39dc7b12ff1649488cb7319ff703d1c1
来源数据集: uspto-grants-2002_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06423689B1
来源说明: uspto-grants-2002_07

反应 SMILES

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