1H-indole-6-carboxylic acid → HCID 21060579, compound

HRID 1241561Notes

Reaction equation

HRID 1241561 reaction equation
Cl.Cl.Cl.Cl.[CH3:5][N:6]1[CH2:11][CH2:10][CH:9]([CH2:12][C@H:13]([C:15]([N:17]2[CH2:22][CH2:21][N:20]([CH:23]3[CH2:28][CH2:27][N:26]([CH3:29])[CH2:25][CH2:24]3)[CH2:19][CH2:18]2)=[O:16])[NH2:14])[CH2:8][CH2:7]1.[NH:30]1[C:38]2[C:33](=[CH:34][CH:35]=[C:36]([C:39](O)=[O:40])[CH:37]=2)[CH:32]=[CH:31]1>>[NH:30]1[C:38]2[C:33](=[CH:34][CH:35]=[C:36]([C:39]([NH:14][C@@H:13]([C:15]([N:17]3[CH2:18][CH2:19][N:20]([CH:23]4[CH2:24][CH2:25][N:26]([CH3:29])[CH2:27][CH2:28]4)[CH2:21][CH2:22]3)=[O:16])[CH2:12][CH:9]3[CH2:10][CH2:11][N:6]([CH3:5])[CH2:7][CH2:8]3)=[O:40])[CH:37]=2)[CH:32]=[CH:31]1

Participants

3

Reactant 2

HCID 5952301H-indole-6-carboxylic acidHCID 21060500HCID 21060500, compound

Product 1

HCID 21060579HCID 21060579, compound

Procedure

Using methods substantially equivalent to those described in Method D-1, the subtitled compound was prepared from 1-[β-(1-methylpiperidin-4-yl)-D-alanyl]-4-(1-methylpiperidin-4-yl)piperazine tetrahydrochloride and indole-6-carboxylic acid (59%).

Sources & evidence

ORD record
ord-7699711b80ff4a17a3a49a91a0cc3d42
Source dataset
uspto-grants-2006_10
Patent number
US07115609B2

Reaction notes

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