HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 18984426, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 18984401 | HCID 18984401 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 18984426 | HCID 18984426 | — |
Reaction Steps
To a mixture of 3-(4-chlorophenyl)-1-[3-(methylamino)propyl]-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one (1.79 g), potassium carbonate (2.18 g) and acetone (50 ml) is added allyl bromide (0.65 g) under ice cooling, and the mixture is stirred at room temperature overnight. The insoluble materials are filtered off and acetone is distilled off, and the oily residue is purified by silica gel column chromatography (eluent, chloroform:methanol=20:1) to give 1-[3-(N-allyl-N-methylamino)propyl]-3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246929 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-0dc1f01a584844b9b9fa0afdb4cd92ab |
| Source note | uspto-grants-1993_09 |