Ammonia → HCID 58981152, compound

HRID 1181778Notes

Reaction equation

HRID 1181778 reaction equation
[CH2:1]([N:5]1[C:10]2=[N:11][N:12]([CH2:23][C:24]3[C:33]4[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=4)[CH:27]=[CH:26][CH:25]=3)[C:13]([C:14]3[CH:15]=[C:16]([CH:20]=[CH:21][CH:22]=3)[C:17]([OH:19])=O)=[C:9]2[C:8](=[O:34])[N:7]([CH3:35])[C:6]1=[O:36])[CH:2]([CH3:4])[CH3:3].[NH3:37]>O>[CH2:1]([N:5]1[C:10]2=[N:11][N:12]([CH2:23][C:24]3[C:33]4[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=4)[CH:27]=[CH:26][CH:25]=3)[C:13]([C:14]3[CH:15]=[C:16]([CH:20]=[CH:21][CH:22]=3)[C:17]([NH2:37])=[O:19])=[C:9]2[C:8](=[O:34])[N:7]([CH3:35])[C:6]1=[O:36])[CH:2]([CH3:4])[CH3:3]

Participants

4

Procedure

This compound was synthesized by the reaction of 3-[7-isobutyl-5-methyl-2-(1-naphthylmethyl)-4,6-dioxo-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-d]pyrimidin-3-yl]benzoic acid and ammonia in water using diethyl isobutyl chloroformate as a coupling reagent Mass: 481.89 (M+H).

Sources & evidence

ORD record
ord-5ef58d048b2048e5a23eb7430ff1d007
Source dataset
uspto-grants-2007_10
Patent number
US07285558B2

Reaction notes

Loading…