HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (2,4-Difluorophenyl)thiocarbamic acid O-(4-hydroxymethyl-5-oxo-2,3,4,5-tetrahydrobenzo[b]thiepin-4-ylmethyl)ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Difluoro-1-isothiocyanatobenzene | HCID 518879 | — |
| Reactant | 4,4-bis(hydroxymethyl)-3,4-dihydro-2H-benzo[b]thiepin-5-one | HCID 67073365 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2,4-Difluorophenyl)thiocarbamic acid O-(4-hydroxymethyl-5-oxo-2,3,4,5-tetrahydrobenzo[b]thiepin-4-ylmethyl)ester | HCID 86633684 | — |
Reaction Steps
To a solution of 4,4-bis(hydroxymethyl)-3,4-dihydro-2H-benzo[b]thiepin-5-one (720 mg, 3.02 mmol) in 38 ml of tetrahydrofuran were added, at room temperature, triethylamine (0.46 ml, 3.32 mmol) and 2,4-difluorophenyl isothiocyanate (985 μl, 7.55 mmol). The mixture was heated to reflux for 72 hours, concentrated and purified by column chromatography on silica gel (eluent: 1:2 ethyl acetate/hexane). The product was obtained in a yield of 170 mg (14%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858613B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-09451c0b23d54413b8e80f90fe217199 |
| Source note | uspto-grants-2010_12 |