HCID 13747415, compound → HCID 13747430, compound

HRID 1034017Notes

Reaction equation

HRID 1034017 reaction equation
[CH2:1]([O:3][C:4]1[CH:19]=[C:18]([CH2:20][C:21]([NH:23][CH:24]([C:37]([O:39][CH2:40][CH2:41][CH3:42])=[O:38])[C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=2[N:31]2[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]2)=[O:22])[CH:17]=[CH:16][C:5]=1[C:6]([O:8]CC1C=CC=CC=1)=[O:7])[CH3:2]>C(O)CC>[CH2:1]([O:3][C:4]1[CH:19]=[C:18]([CH2:20][C:21]([NH:23][CH:24]([C:37]([O:39][CH2:40][CH2:41][CH3:42])=[O:38])[C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=2[N:31]2[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]2)=[O:22])[CH:17]=[CH:16][C:5]=1[C:6]([OH:8])=[O:7])[CH3:2]

Participants

3

Reactant 1

HCID 13747415HCID 13747415, compound

Product 1

HCID 13747430HCID 13747430, compound

Reagents, catalysts & solvents 1

HCID 10311-PropanolSolvent

Procedure

Prepared analogously to Example 40 by catalytic hydrogenation of benzyl 2-ethoxy-4-[N-(α-n-propoxycarbonyl-2-piperidino-benzyl)-aminocarbonylmethyl]-benzoate in n-propanol.

Sources & evidence

ORD record
ord-e910f2d2d4be48e3ab3e0a737f339306
Source dataset
uspto-grants-1994_05
Patent number
US05312924

Reaction notes

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