Succinimide → HCID 66616516, compound

HRID 538710Notes

Reaction equation

HRID 538710 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([C:17]2[C:18]([CH3:34])([CH3:33])[C:19](=[O:32])[N:20]([CH:22]3[CH2:27][CH2:26][N:25]([C:28](=[O:31])[CH2:29]Cl)[CH2:24][CH2:23]3)[N:21]=2)[CH:12]=[CH:13][C:14]=1[O:15][CH3:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:35]1(=[O:41])[NH:39][C:38](=[O:40])[CH2:37][CH2:36]1>>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([C:17]2[C:18]([CH3:34])([CH3:33])[C:19](=[O:32])[N:20]([CH:22]3[CH2:27][CH2:26][N:25]([C:28](=[O:31])[CH2:29][N:39]4[C:35](=[O:41])[CH2:36][CH2:37][C:38]4=[O:40])[CH2:24][CH2:23]3)[N:21]=2)[CH:12]=[CH:13][C:14]=1[O:15][CH3:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 11439SuccinimideHCID 66616671HCID 66616671, compound

Product 1

HCID 66616516HCID 66616516, compound

Procedure

Prepared analogously as described for example 1 using 5-[3-(benzyloxy)-4-methoxyphenyl]-2-[1-(chloroacetyl)piperidin-4-yl]-4,4-dimethyl-2,4-dihydro-3H-pyrazol-3-one (see below) and succinimide as starting compounds.

Workup

  1. customPrepared analogously

Sources & evidence

ORD record
ord-909664b99d89483f8cc4bbf6fb5d1193
Source dataset
uspto-grants-2014_10
Patent number
US08865745B2

Reaction notes

Loading…