Piperidin-4-ol → HCID 59077510, compound

HRID 1359790Notes

Reaction equation

HRID 1359790 reaction equation
O=C1CCC(=O)N1[O:8][C:9]([C:11]1[C:15]([CH3:16])=[C:14](/[CH:17]=[C:18]2\[C:19](=[O:39])[NH:20][C:21]3[C:26]\2=[CH:25][C:24]([S:27]([CH2:30][C:31]2[CH:36]=[C:35]([Cl:37])[CH:34]=[CH:33][C:32]=2[Cl:38])(=[O:29])=[O:28])=[CH:23][CH:22]=3)[NH:13][C:12]=1[CH3:40])=O.[NH:41]1[CH2:46][CH2:45][CH:44]([OH:47])[CH2:43][CH2:42]1>>[Cl:38][C:32]1[CH:33]=[CH:34][C:35]([Cl:37])=[CH:36][C:31]=1[CH2:30][S:27]([C:24]1[CH:25]=[C:26]2[C:21](=[CH:22][CH:23]=1)[NH:20][C:19](=[O:39])/[C:18]/2=[CH:17]\[C:14]1[NH:13][C:12]([CH3:40])=[C:11]([C:9]([N:41]2[CH2:46][CH2:45][CH:44]([OH:47])[CH2:43][CH2:42]2)=[O:8])[C:15]=1[CH3:16])(=[O:29])=[O:28]

Participants

3

Reactant 2

HCID 79341Piperidin-4-olHCID 88095587HCID 88095587, compound

Product 1

HCID 59077510HCID 59077510, compoundYield 25.5%

Procedure

5-[5-(2,5-Dichloro-phenylmethanesulfonyl)-2-oxo-1,2-dihydro-indol-(3Z)-ylidenemethyl]-2,4-dimethyl-1H-pyrrole-3-carboxylic acid 2,5-dioxo-pyrrolidin-1-yl ester (120 mg, 0.2 mmol) was condensed with piperidin-4-ol (21 mg, 0.2 mmol) to give 30 mg the titled compound.

Sources & evidence

ORD record
ord-bee69ad892984434b7396ea19d6bab9f
Source dataset
uspto-grants-2003_07
Patent number
US06599902B2

Reaction notes

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