Maleic Acid → HCID 131711357, compound
Reaction equation
[C:1]1([CH:7]2[N:12]3[CH2:13][CH2:14][S:15][C:11]3=[N:10][C:9]3[C:16](=[CH:20][C:21]4[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=4)[CH2:17][S:18][CH2:19][C:8]2=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:27]([OH:34])(=[O:33])/[CH:28]=[CH:29]\[C:30]([OH:32])=[O:31]>CO>[C:27]([OH:34])(=[O:33])/[CH:28]=[CH:29]\[C:30]([OH:32])=[O:31].[C:1]1([CH:7]2[N:12]3[CH2:13][CH2:14][S:15][C:11]3=[N:10][C:9]3[C:16](=[CH:20][C:21]4[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=4)[CH2:17][S:18][CH2:19][C:8]2=3)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of 2,3,8,9-tetrahydro-5-phenyl-9-(phenylmethylene)-5H,6H-thiazolo[3,2-a]thiopyrano[4,3-d]pyrimidine (3.0 g, 0.0079 mole) in 25 ml of MeOH is treated with 0.92 g (0.0079 mole) of maleic acid. The solution is evaporated in vacuo to give an oil which gradually solidifies. The yield is 3.7 g, m.p. 142°-144°. Crystallization from 15 ml of MeCN gives 3.0 g (77%) of cream colored product, m.p. 143°-145°.
Workup
- customThe solution is evaporated in vacuo
- customto give an oil which
- customCrystallization from 15 ml of MeCN
- customgives 3.0 g (77%) of cream colored product, m.p. 143°-145°
Sources & evidence
- ORD record
- ord-521b210dea4649c4b26775bb00b2e438
- Source dataset
- uspto-grants-1978_12
- Patent number
- US04128647
Reaction notes
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