4,6-Dioxo-10-propyl-4H,6H-benzo(1,2-b:5,4-b')dipyran-2,8-dicarboxylic acid → HCID 131712429, compound
Reaction equation
[O:1]=[C:2]1[CH:7]=[C:6]([C:8]([OH:10])=[O:9])[O:5][C:4]2[C:11]([CH2:23][CH2:24][CH3:25])=[C:12]3[C:17](=[CH:18][C:3]1=2)[C:16](=[O:19])[CH:15]=[C:14]([C:20]([OH:22])=[O:21])[O:13]3.C(=O)([O-])[O-].[NH2:30][C:31]([NH2:33])=[NH2+:32].[NH2:34][C:35]([NH2:37])=[NH2+:36]>O>[NH2:32][C:31]([NH2:33])=[NH2+:30].[NH2:36][C:35]([NH2:37])=[NH2+:34].[O:19]=[C:16]1[CH:15]=[C:14]([C:20]([O-:22])=[O:21])[O:13][C:12]2[C:11]([CH2:23][CH2:24][CH3:25])=[C:4]3[C:3](=[CH:18][C:17]1=2)[C:2](=[O:1])[CH:7]=[C:6]([C:8]([O-:10])=[O:9])[O:5]3Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4,6-Dioxo-10-propyl-4H,6H-benzo[1,2-b:5,4-b']dipyran-2,8-dicarboxylic acid (1.0 g) was added to a stirred solution of guanidinium carbonate (0.52 g) in water (20 ml) and the mixture was stirred at room temperature until effervescence had ceased. The precipitated solid was collected using a centrifuge, washed with water and acetone and dried in vacuo at 70° C. to give the title compound (0.83 g; 62%).
Workup
- customThe precipitated solid was collected
- washwashed with water and acetone
- customdried in vacuo at 70° C.
Sources & evidence
- ORD record
- ord-9bd503af679c4e8098bc16607c14d1cd
- Source dataset
- uspto-grants-1981_10
- Patent number
- US04293541
Reaction notes
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