HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 4-[3-(6-Bromopyridin-3-yl)propyl]thiomorpholin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,4-Tetrahydrothiazine-3-one | HCID 88402 | — |
| Reactant | 2-Bromo-5-(3-bromopropyl)pyridine | HCID 71427771 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[3-(6-Bromopyridin-3-yl)propyl]thiomorpholin-3-one | HCID 71427770 | — |
Reaction Steps
60.2 mg (1.38 mmol) of sodium hydride (55% suspension in mineral oil) were added to 161.7 mg (1.38 mmol) of thiomorpholin-3-one in 5 ml of DMF, and the mixture was stirred at room temperature for 15 min. Subsequently, 350 mg (1.25 mmol) of 2-bromo-5-(3-bromopropyl)pyridine were added. The reaction mixture was stirred for 3.5 h, concentrated, admixed with water and extracted with ethyl acetate. The organic phase was separated and concentrated. Yield: 421 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518976B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-c3a1979e7db34a9cbabcf372a0f085e5 |
| Source note | uspto-grants-2013_08 |