Hydrochloric Acid → HCID 13559271, compound
Reaction equation
[C:1]([S:4][CH2:5][C:6]1[NH:7][C:8]([CH3:32])=[C:9]([C:27]([O:29][CH2:30][CH3:31])=[O:28])[CH:10]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[C:23]([F:26])([F:25])[F:24])[C:11]=1C(OCC)=O)(=[O:3])C.Cl>C(O)C>[CH3:32][C:8]1[NH:7][C:6]2[CH2:5][S:4][C:1](=[O:3])[C:11]=2[CH:10]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[C:23]([F:26])([F:25])[F:24])[C:9]=1[C:27]([O:29][CH2:30][CH3:31])=[O:28]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
10 mmol of diethyl 2 -acetylthiomethyl-6-methyl-4-(2-trifluoromethylphenyl)-1,4-dihydropyridine-3,5-dicarboxylate, dissolved in 40 ml of ethanol, are boiled with 6 ml of saturated ethanolic HCl for 2 hours and the product is precipitated with water and then recrystallized from ethanol.
Workup
- customthe product is precipitated with water
- customrecrystallized from ethanol
Sources & evidence
- ORD record
- ord-7d87f6a503a843b39c31b0219576c861
- Source dataset
- uspto-grants-1987_02
- Patent number
- US04642310
Reaction notes
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