Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 7-Fluoro-2-methylsulfonyl-1,3-benzothiazole | HCID 19391745 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Fluoro-1,3-benzothiazol-2-amine | HCID 14892245 | — |
Reaction Steps
A mixture of 7-fluoro-2-methylsulfonyl-1,3-benzothiazole (500 mg, 2.16 mmol) in 10 mL ethanol and 20% ethanolic ammonia (20 mL) was heated at 160° C. in a sealed tube for 12 h. It was cooled to RT, ethanol was removed under reduced pressure, and the brownish residue was purified by column chromatography (5% to 10% methanol in methylene chloride) to afford the title compound. 1H-NMR (CDCl3, 300 MHz): δ=7.35 (d, J=7.5 Hz, 1H), 7.33-7.37 (m, 1H), 6.93-6.84 (m, 1H), 5.30 (brs, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08178668B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-fbd7008f0aec4d6c826646992077952a |
|---|
| Source note | uspto-grants-2012_05 |
|---|