6-Chloro-1-benzothiophene-2-carboxylic acid → HCID 69597391, compound

HRID 1241564Notes

Reaction equation

HRID 1241564 reaction equation
Cl.Cl.Cl.[NH2:4][C@@H:5]([C:10]([N:12]1[CH2:17][CH2:16][N:15]([CH:18]2[CH2:23][CH2:22][N:21]([CH3:24])[CH2:20][CH2:19]2)[CH2:14][CH2:13]1)=[O:11])[CH2:6][C:7](=[O:9])[NH2:8].[Cl:25][C:26]1[CH:27]=[CH:28][C:29]2[CH:33]=[C:32]([C:34](O)=[O:35])[S:31][C:30]=2[CH:37]=1>>[Cl:25][C:26]1[CH:27]=[CH:28][C:29]2[CH:33]=[C:32]([C:34]([NH:4][C@@H:5]([C:10]([N:12]3[CH2:17][CH2:16][N:15]([CH:18]4[CH2:19][CH2:20][N:21]([CH3:24])[CH2:22][CH2:23]4)[CH2:14][CH2:13]3)=[O:11])[CH2:6][C:7](=[O:9])[NH2:8])=[O:35])[S:31][C:30]=2[CH:37]=1

Participants

3

Procedure

Using methods substantially equivalent to those described in Method D-1, the subtitled compound was prepared from 1-(D-asparaginyl)-4-(1-methylpiperidin-4-yl)piperazine trihydrochloride and 6-chlorobenzo[b]thiophene-2-carboxylic acid (40%).

Sources & evidence

ORD record
ord-ea369755aec94fd58e3dd89815855b6f
Source dataset
uspto-grants-2006_10
Patent number
US07115609B2

Reaction notes

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