HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → 3-Amino-5-bromo-1-methyl-1,2-dihydropyridin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 5-bromo-3-(diphenylmethyleneamino)-1-methylpyridin-2(1H)-one | HCID 86684584 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Amino-5-bromo-1-methyl-1,2-dihydropyridin-2-one | HCID 52911268 | 52.1% |
Reaction Steps
To a solution of 5-bromo-3-(diphenylmethyleneamino)-1-methylpyridin-2(1H)-one (3.82 g, 10.4 mmol) in ethyl acetate (10 mL) was added 4 MHCl/dioxane (7.8 mL, 31.3 mmol). The reaction mixture was stirred for 0.5 h and concentrated under reduced pressure. The residue was washed with tert-butyl methyl ether and filtered. The solid was dissolved in ethyl acetate (10 mL) and water (10 mL). The pH of the resulting mixture was adjusted to between 7 and 8 by adding K2CO3 gradually. The water phase was separated and extracted with dichloromethane for three times. The combined organic layer was concentrated under reduced pressure to afford 325a as a yellow solid (1.1 g, 52%). MS-ESI: [M+H]+ 202.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238655B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-9ff511ce15504abbb20a28f791ce8a61 |
| Source note | uspto-grants-2016_01 |