HRID383167

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2724685

9H-Fluoren-9-amine hydrochloride

C13H12ClN

结构：COC(=O)[C@H](CCSC)NC(=O)c1ccc(C=O)cc1-c1ccccc1C

HCID10596254

未命名化合物

PRODUCTS

生成物

结构：COC(=O)[C@H](CCSC)NC(=O)c1ccc(CNC2c3ccccc3-c3ccccc32)cc1-c1ccccc1C

HCID70210817

未命名化合物

PROCEDURE

实验过程

The desired compound was prepared using the method described in Example 403H starting with N-[4-formyl-2-(2-methylphenyl)benzoyl]methionine methyl ester, prepared as in Example 403G, and 9-aminofluorene hydrochloride salt m/e (ESI) 551 (MH+)

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-ea21751830674f9bb21e0d3802af75e1
来源数据集: uspto-grants-2001_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06310095B1
来源说明: uspto-grants-2001_10

反应 SMILES

[CH3:1][O:2][C:3](=[O:27])[C@H:4]([CH2:23][CH2:24][S:25][CH3:26])[NH:5][C:6](=[O:22])[C:7]1[CH:12]=[CH:11][C:10]([CH:13]=O)=[CH:9][C:8]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH3:21].Cl.[NH2:29][CH:30]1[C:42]2[CH:41]=[CH:40][CH:39]=[CH:38][C:37]=2[C:36]2[C:31]1=[CH:32][CH:33]=[CH:34][CH:35]=2>>[CH3:1][O:2][C:3](=[O:27])[C@H:4]([CH2:23][CH2:24][S:25][CH3:26])[NH:5][C:6](=[O:22])[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][NH:29][CH:30]2[C:42]3[CH:41]=[CH:40][CH:39]=[CH:38][C:37]=3[C:36]3[C:31]2=[CH:32][CH:33]=[CH:34][CH:35]=3)=[CH:9][C:8]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH3:21]