Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,3-Propanesultam | HCID 642157 | — |
| Reactant | HCID 20266386 | HCID 20266386 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20266398 | HCID 20266398 | — |
Reaction Steps
Sodium hydride (1.25 g of a 50% dispersion in oil) was added at room temperature to a stirred solution of isothiazolidine-1,1-dioxide (2.42 g) in DMF (15 cm3). After stirring for 0.5 hours 2-methyl-2-[1-(6,7-dimethoxyquinazolin-4-yl)piperid-4-yl]oxirane (5.0 g) was added and the mixture was stirred for 4 hours at 100°. Volatile material was removed in vacuo, the residue was partitioned between chloroform (100 cm3) and water (50 cm3) and the chloroform layer was dried (MgSO4) and evaporated. The residue was chromatographed on silica ("Merck" 60.9385) eluting with methanol:ethyl acetate, 1:4, to give a solid which was recrystallised from ethyl acetate-methanol to give 2-{2-hydroxy-2-[1-(6,7-dimethoxyquinazolin-4-yl)piperid-4-yl]prop-1-yl}isothiazolidine-1,1-dioxide, m.p. 173°-174° (4.15 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04542132 |
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| Source dataset | uspto-grants-1985_09 |
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| ORD ID | ord-0ac898f11f384d3ab3f3ae727bbdc046 |
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| Source note | uspto-grants-1985_09 |
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