HCID 19602866, compound → HCID 19602690, compound

HRID 1604340Notes

Reaction equation

HRID 1604340 reaction equation
[ClH:1].Cl.[C:3]([CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][CH:22]3[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]3)[CH2:16][CH2:15]2)=[CH:10][CH:9]=1)([OH:5])=[O:4]>C(O)CCC>[ClH:1].[ClH:1].[CH2:13]([O:4][C:3]([CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][CH:22]3[CH2:23][CH2:24][NH:25][CH2:26][CH2:27]3)[CH2:16][CH2:15]2)=[CH:10][CH:9]=1)=[O:5])[CH2:8][CH2:9][CH3:10]

Participants

3

Procedure

Prepared from 1-(4-carboxymethyloxyphenyl)-4-[2-(piperidin-4-yl)ethyl]piperazine dihydrochloride and n-butanol.

Sources & evidence

ORD record
ord-7072b394753a4c24b4eb9b3791286396
Source dataset
uspto-grants-1999_11
Patent number
US05994356

Reaction notes

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