(R)-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyril → (r)-3-(5-Chloroindole-2-carbonylamino)-1-cyanomethyl-3,4-dihydrocarbostyril

HRID 11590

Reaction equation

HRID 11590 reaction equation
ClC1C=C2C(=CC=1)NC(C(N[C@@H]1CC3C(=CC=CC=3)NC1=O)=O)=C2.[Cl:25][C:26]1[CH:27]=[C:28]2[C:32](=[CH:33][CH:34]=1)[NH:31][C:30]([C:35]([NH:37][C@H:38]1[CH2:47][C:46]3[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=3)[N:40]([CH2:48][C:49]#[N:50])[C:39]1=[O:51])=[O:36])=[CH:29]2.ClC1C=C2C(=CC=1)NC(C(N[C@H]1CC3C(=CC=CC=3)NC1=O)=O)=C2>>[Cl:25][C:26]1[CH:27]=[C:28]2[C:32](=[CH:33][CH:34]=1)[NH:31][C:30]([C:35]([NH:37][C@@H:38]1[CH2:47][C:46]3[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=3)[N:40]([CH2:48][C:49]#[N:50])[C:39]1=[O:51])=[O:36])=[CH:29]2

Participants

4

Procedure

The title compound was prepared from (R)-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyril (Example 3) by the procedures described for the preparation of (S)-3-(5-chloroindole-2-carbonylamino)-1-cyanomethyl-3,4-dihydrocarbostyril (Example 17) from (S)-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyril. HPLC/MS [M+H]+, 379.

Sources & evidence

ORD record
ord-b00a7ed4fdea484c9fcb5f3121dbfe6d
Source dataset
uspto-grants-2006_08
Patent number
US07098235B2

Linked notes

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