HRID412456

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7150

Methyl benzoate

C8H8O2

HCID263366

1-([1,1'-Biphenyl]-2-yl)methanamine

C13H13N

结构：COC(=O)c1ccc(CN(C(=O)NCl)c2ccc(C3CCCCC3)cc2)cc1

HCID86586062

未命名化合物

HCID86586063

未命名化合物

PRODUCTS

生成物

结构：O=C(NC[C@@H](O)C(=O)O)c1ccc(CN(C(=O)NCc2ccccc2-c2ccccc2)c2ccc(C3CCCCC3)cc2)cc1

HCID10258106

未命名化合物

PROCEDURE

实验过程

This compound was prepared similarly as described in example 35 from N-chlorocarbamoyl-4-[(4-cyclohexylphenylamino)methyl]benzoic acid methyl ester and biphenyl-2-ylmethylamine followed by hydrolysis of the benzoic acid methyl ester, coupling with (R)-isoserine ethyl ester hydrochloride. Hydrolysis afforded the title compound.

WORKUP

后处理

customThis compound was prepared similarly
customHydrolysis

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-de5d1ad0dcf94b3684155d7172a7e1b6
来源数据集: uspto-grants-2003_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06562807B2
来源说明: uspto-grants-2003_05

反应 SMILES

CO[C:3](=[O:28])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][N:11]([C:16]2[CH:21]=[CH:20][C:19]([CH:22]3[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]3)=[CH:18][CH:17]=2)[C:12](=[O:15])[NH:13]Cl)=[CH:6][CH:5]=1.[C:29]1([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=1[CH2:35]N.COC(=O)C1C=CC=CC=1.Cl.C([O:56][C:57](=[O:62])[C@H:58]([OH:61])[CH2:59][NH2:60])C>>[C:29]1([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=1[CH2:35][NH:13][C:12](=[O:15])[N:11]([CH2:10][C:7]1[CH:6]=[CH:5][C:4]([C:3]([NH:60][CH2:59][C@@H:58]([OH:61])[C:57]([OH:62])=[O:56])=[O:28])=[CH:9][CH:8]=1)[C:16]1[CH:21]=[CH:20][C:19]([CH:22]2[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]2)=[CH:18][CH:17]=1