Malonic Acid → HCID 178443390, compound
Reaction equation
C(O)(=O)C.[CH3:5][C:6]1([CH3:33])[N:11]=[C:10]([NH:12][CH2:13][C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)[NH:9][C:8]([NH:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[N:7]1.[C:34]([OH:40])(=[O:39])[CH2:35][C:36]([OH:38])=[O:37]>C(#N)C>[C:34]([OH:40])(=[O:39])[CH2:35][C:36]([OH:38])=[O:37].[CH3:5][C:6]1([CH3:33])[N:11]=[C:10]([NH:12][CH2:13][C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)[NH:9][C:8]([NH:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])=[N:7]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3.0 g (7.5 mmol) of the compound (1) of Working Example 38 was dissolved in 30 ml of 70% aqueous acetonitrile, and to the solution was added 0.85 g (8.17 mmol) of malonic acid. The mixture was dissolved by heating, and then cooled to obtain 3.0 g of colorless crystals having a melting point of 109 to 112° C.
Workup
- dissolutionThe mixture was dissolved
- temperatureby heating
- temperaturecooled
Sources & evidence
- ORD record
- ord-ecd4cbd6cb5d4028be8f696cda34dd0e
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07622469B2
Reaction notes
Loading…