HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 20266409, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20266408 | HCID 20266408 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20266409 | HCID 20266409 | — |
Reaction Steps
Sodium borohydride (40 mg) was added at 0° to a stirred solution of 2-{2-oxo-2-[1-(6,7-dimethoxyquinazolin-4-yl)piperid-4-yl]ethyl}-5-methyl-1,2,6-thiadiazine-1,1-dioxide (0.4 g) in ethanol (10 cm3). After 2 hours the volatile material was removed in vacuo and the residue was partitioned between water (10 cm3) and dichloromethane (20 cm3). The dried organic extract was evaporated to give a solid which was chromatographed on silica ("Merck" 60.9385) eluting with methanol:chloroform, 1:19, to give a foam which was crystallised from ethyl acetate to afford 2-{2-hydroxy-2-[1-(6,7-dimethoxyquinazolin-4-yl)piperid-4-yl]ethyl}-5-methyltetrahydro-1,2,6-thiadiazine-1,1-dioxide as microcrystals, m.p. 189°-193° (0.30 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04542132 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-25ba1cfb4dcd4dbd835938ce7afebb7a |
| Source note | uspto-grants-1985_09 |