Sulfuric Acid → HCID 13100542, compound
Reaction equation
S(=O)(=O)(O)O.[NH2:6][C:7]1[C:16]2[C:11](=[C:12]([O:20][CH3:21])[C:13]([O:18][CH3:19])=[C:14]([Cl:17])[CH:15]=2)[N:10]=[C:9]([N:22]2[CH2:27][CH2:26][N:25]([C:28]([O:30][CH2:31][C:32](=[CH2:34])[CH3:33])=[O:29])[CH2:24][CH2:23]2)[N:8]=1.[OH-:35].[Na+]>O>[NH2:6][C:7]1[C:16]2[C:11](=[C:12]([O:20][CH3:21])[C:13]([O:18][CH3:19])=[C:14]([Cl:17])[CH:15]=2)[N:10]=[C:9]([N:22]2[CH2:27][CH2:26][N:25]([C:28]([O:30][CH2:31][C:32]([CH3:33])([OH:35])[CH3:34])=[O:29])[CH2:24][CH2:23]2)[N:8]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirred solution of 24 ml. of concentrated sulfuric acid dissolved in an equal volume of water was cooled to 10°-12° C. and 0.015 mole of methallyl 4-(4-amino-6-chloro-7,8-dimethoxyquinazolin-2-yl)-piperazine-1-carboxylate is added in small portions with stirring. The addition is carried out at a rate sufficient to keep the reaction temperature below 20° C. The resulting mixture is stirred for 15 minutes at 15°-20° C., then for two hours at 10°-15° C. The reaction mixture is diluted with 150 ml. of ice-water and adjusted to pH 10 with sodium hydroxide while maintaining the temperature below 12° C. After extraction with chloroform, the combined extracts are washed with water and dried over anhydrous sodium sulfate. The solvent is evaporated in vacuo and the residue recrystallized to afford 2-methyl-2-hydroxypropyl 4-(4-amino-6-chloro-7,8-dimethoxyquinazolin-2-yl)piperazine-1-carboxylate.
Workup
- temperaturewas cooled to 10°-12° C.
- additionThe addition
- customthe reaction temperature below 20° C
- stirringThe resulting mixture is stirred for 15 minutes at 15°-20° C.
- additionThe reaction mixture is diluted with 150 ml
- temperaturewhile maintaining the temperature below 12° C
- extractionAfter extraction with chloroform
- washthe combined extracts are washed with water
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent is evaporated in vacuo
- customthe residue recrystallized
Sources & evidence
- ORD record
- ord-bb9de7c7f21e460ba7a94af62eb7203c
- Source dataset
- uspto-grants-1983_03
- Patent number
- US04377581
Reaction notes
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