反応 #316284

ord-a12bdece37424bf3b6d13861d9a09008

反応方程式

C[C@H](CNCC(c1ccccc1)c1ccccc1)COc1cccc(CC(=O)O)c1
(R)-2-(3-{3-[(2,2-diphenylethyl)amino]2-methyl-propoxy}-phenyl)acetic acid
COC(C)=O
acetic acid methyl ester
O=Cc1cccc(C(F)(F)F)c1Cl
2-chloro-3-trifluoromethylbenzaldehyde
CCOCC.Cl
HCl Et2O
COc1ccc(C=O)c(F)c1
2-fluoro-4-methoxybenzaldehyde
COc1ccc(CN(CC(c2ccccc2)c2ccccc2)C[C@@H](C)COc2cccc(CC(=O)O)c2)c(F)c1.Cl
title compound
COc1ccc(CN(CC(c2ccccc2)c2ccccc2)C[C@@H](C)COc2cccc(CC(=O)O)c2)c(F)c1.Cl
(R)-2-(3-{3-[[2-Fluoro-4-methoxy-benzyl](2,2-diphenylethyl)amino]-2-methyl-propoxy}-phenyl)acetic acid hydrochloride salt

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他was obtained
  2. 2
    濃縮The reaction mixture was concentrated in vacuo
  3. 3
    その他dried under reduced pressure

実験手順

Following the procedure of Example 7(d) except (R)-2-(3-{3-[(2,2-diphenylethyl)amino]2-methyl-propoxy}-phenyl)acetic acid and 2-fluoro-4-methoxybenzaldehyde were used instead of (R)-2-(3-{3-(2,2-diphenylethyl)amino]-3-methyl-propoxy}-phenyl)acetic acid methyl ester and 2-chloro-3-trifluoromethylbenzaldehyde in step (d) the corresponding carboxylic acid was obtained. The resulting amine/carboxylic acid was dissolved in Et2O (diethylether) and acidified with 1.0 M HCl/Et2O. The reaction mixture was concentrated in vacuo and dried under reduced pressure to give the title compound as a white solid, 98 mg (98%). MS (ESI) 542.4 (M+H+).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07560586B2uspto-grants-2009_07