HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl isothiocyanate → 1-(2-Amino-benzothiazol-5-yl)-3-benzoyl-thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | 1,3-Benzothiazole-2,5-diamine | HCID 768525 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Amino-benzothiazol-5-yl)-3-benzoyl-thiourea | HCID 10042159 | — |
Reaction Steps
To a solution of anhydrous THF (6.7 mL) was added 5-amino-benzothiazol-2-ylamine (Example 16, 100 mg, 0.61 mmol) and benzoyl isothiocyanate (0.08 mL, 1 equiv). The resulting mixture was stirred at room temperature for 2 hours, after which the solvent was evaporated and the residue was washed with a 1:1 mixture of ether/hexanes (0.164 g, 83%). 1H NMR (DMSO d6) δ: 12.61 (s, 1H), 11.53 (s, 1H), 7.99 (d, 1H, J=3.9 Hz), 7.76 (s, 1H), 7.69–7.65 (m, 2H), 7.59–7.53 (m, 4H), 7.25–7.23 (d, 1H, J=3.9 Hz); MS (ESI) 328.8 (M+1, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07141595B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-1afc06bd929541f28f03a93a0aca4b46 |
| Source note | uspto-grants-2006_11 |