Sodium hydride → HCID 20434952, compound
Reaction equation
[H-].[Na+].[S:3]1(=[O:10])(=[O:9])[N:8]=[CH:7][CH:6]=[CH:5][NH:4]1.[CH3:11][O:12][C:13]1[CH:14]=[C:15]2[C:20](=[CH:21][C:22]=1[O:23][CH3:24])[N:19]=[CH:18][N:17]=[C:16]2[N:25]1[CH2:30][CH2:29][CH:28]([CH2:31][CH2:32]Br)[CH2:27][CH2:26]1>CN(C)C=O>[CH3:11][O:12][C:13]1[CH:14]=[C:15]2[C:20](=[CH:21][C:22]=1[O:23][CH3:24])[N:19]=[CH:18][N:17]=[C:16]2[N:25]1[CH2:30][CH2:29][CH:28]([CH2:31][CH2:32][N:8]2[CH:7]=[CH:6][CH:5]=[N:4][S:3]2(=[O:10])=[O:9])[CH2:27][CH2:26]1Participants
Procedure
Sodium hydride (0.19 g. of a 50% dispersion in oil) was added to a stirred solution of 2H-1,2,6-thiadiazine-1,1-dioxide (0.52 g) in dimethylformamide (4 cm3). After 0.5 hours 1-(6.7-dimethoxyquinazolin-4-yl)-4-(2-bromoethyl)piperidine (0.60 g) was added and the mixture was warmed at 70° for 10 hours. The solvent was removed in vacuo, water was added and the mixture was extracted with chloroform (4×20 cm3). The dried (MgSO4) extracts were evaporated and the residue was chromatographed on silica (Merck 60. 9385) eluting with methanol:ethyl acetate, 1:19, to give an oil which was crystallised from ethyl acetate to afford 1-(6,7-dimethoxyquinazolin-4-yl)-4-[2-(1,1-dioxo-1,2,6-thiadiazin-2-yl)ethyl]piperidine as microcrystals, m.p. 176°-8°, (0.18 g).
Workup
- temperaturethe mixture was warmed at 70° for 10 hours
- customThe solvent was removed in vacuo, water
- additionwas added
- extractionthe mixture was extracted with chloroform (4×20 cm3)
- dry with materialThe dried (MgSO4) extracts
- customwere evaporated
- customthe residue was chromatographed on silica (Merck 60. 9385)
- washeluting with methanol
- customethyl acetate, 1:19, to give an oil which
- customwas crystallised from ethyl acetate
Sources & evidence
- ORD record
- ord-a9713af738994d63838183ff6bfca1c3
- Source dataset
- uspto-grants-1984_12
- Patent number
- US04489075
Reaction notes
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