HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl isothiocyanate → HCID 10414012, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | HCID 21878492 | HCID 21878492 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10414012 | HCID 10414012 | 95% |
Reaction Steps
N2-[2-(4-Bromo-phenyl)-ethyl]-benzothiazole-2,6-diamine (Example 33(a), 71 mg, 0.205 mmol) was dissolved in tetrahydrofuran (3 mL). Benzoyl isothiocyanate (20 μl, 1.1 eq) was added and the mixture stirred at room temperature for 24 hours. The solvent was evaporated to give a yellow solid. The solid was dissolved in CH2Cl2 (5 mL) and absorbed onto silica gel. The absorbed compound was loaded onto a silica column and eluted with a mixture of ethyl acetate/hexanes (1:1) to give a yellow solid (99 mg, 95%). 1H NMR (CDCl3) δ: 12.61 (s, 1H), 9.10 (s, 1H), 8.19 (s, 1H), 7.90 (d, 2H, J=8.5 Hz), 7.67–7.43 (m, 8H), 7.12 (d, 2H, J=8.5 Hz), 3.69 (t, 2H, J=6.9 Hz), 2.97 (d, 2H, J=6.9 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07141595B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-7239a82f1ad34d478a1cb85d7a0ab09d |
| Source note | uspto-grants-2006_11 |