HRID1261420

反应详情

EQUATION

反应方程式

REACTANTS

反应物

$结构：O=C(O)CCC/C=C\C[C@@H]1[C@@H](/C=C/[C@@H](O)COc2cccc(C(F)(F)F)c2)[C@H](O)C[C@@H]1O$

HCID5311100

(±)-Fluprostenol

C23H29F3O6

HCID178512822

未命名化合物

PRODUCTS

生成物

$结构：CC(C)OC(=O)CCC/C=C\C[C@@H]1[C@@H](/C=C/[C@@H](O)COc2cccc(C(F)(F)F)c2)[C@H](O)C[C@@H]1O.N=C(N)NCCCC[C@H](N)C(=O)O$

HCID178459548

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID22242641

Methanol--water (1/1)

CH6O2

PROCEDURE

实验过程

To travoprost free acid ((+)-fluprostenol free acid) 3 in MeOH/H2O is added L-Homoarginine and the solution is stirred for 30 minutes. The solvents are evaporated then azeotroped with Et2O and hexanes to give white crystalline travoprost-L-Homoarginine salt 5 (quantitative).

WORKUP

后处理

customThe solvents are evaporated
customthen azeotroped with Et2O and hexanes

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-ea7ed4de493b4e27ad863e5c6c39af35
来源数据集: uspto-grants-2013_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08470882B2
来源说明: uspto-grants-2013_06

反应 SMILES

[CH2:1]1[C@@H:5]([OH:6])[C@H:4](/[CH:7]=[CH:8]/[C@@H:9]([OH:22])[CH2:10][O:11][C:12]2[CH:17]=[C:16]([C:18]([F:21])([F:20])[F:19])[CH:15]=[CH:14][CH:13]=2)[C@@H:3]([CH2:23]/[CH:24]=[CH:25]\[CH2:26][CH2:27][CH2:28][C:29]([OH:31])=[O:30])[C@H:2]1[OH:32].[NH2:33][C@H:34]([C:43]([OH:45])=[O:44])[CH2:35][CH2:36][CH2:37][CH2:38][NH:39][C:40]([NH2:42])=[NH:41]>CO.O>[CH3:35][CH:34]([O:30][C:29]([CH2:28][CH2:27][CH2:26]/[CH:25]=[CH:24]\[CH2:23][C@@H:3]1[C@@H:4](/[CH:7]=[CH:8]/[C@@H:9]([OH:22])[CH2:10][O:11][C:12]2[CH:13]=[CH:14][CH:15]=[C:16]([C:18]([F:21])([F:20])[F:19])[CH:17]=2)[C@H:5]([OH:6])[CH2:1][C@@H:2]1[OH:32])=[O:31])[CH3:43].[NH2:33][C@H:34]([C:43]([OH:45])=[O:44])[CH2:35][CH2:36][CH2:37][CH2:38][NH:39][C:40]([NH2:42])=[NH:41]