HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Ethyl 2-(carbamothioylamino)-4,5-dimethylthiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethyl 2-isothiocyanato-4,5-dimethylthiophene-3-carboxylate | HCID 3419522 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(carbamothioylamino)-4,5-dimethylthiophene-3-carboxylate | HCID 777992 | 3% |
Reaction Steps
To a solution of ethyl 2-isothiocyanato-4,5-dimethylthiophene-3-carboxylate (Example 50b) (1.21 g, 5.27 mmol) in dichloromethane (10 mL) was added ammonia (7 M in MeOH, 1.12 mL, 7.91 mmol) at 0° C. The reaction mixture was then stirred at room temperature for 3 h, quenched with water and extracted with dichloromethane (3×). The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated. The dark orange residue was purified by chromatography on silica gel (Gradient 0-50% EtOAc in Hexanes) to give the title compound (37.1 mg, 3%). 1H NMR (400 MHz, DMSO-d6) δ 1.32 (t, 3H, J=7.1 Hz), 2.18 (s, 3H), 2.19 (s, 3H), 4.30 (q, 2H, J=7.1 Hz), 8.43 (s, 2H), 11.38 (s, 1H). MS 259 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633186B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-647731cea6f84fd8b1b8b3724fee061f |
| Source note | uspto-grants-2014_01 |