HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl isothiocyanate → 1-Benzoyl-3-(3-(benzyloxy)-5-bromopyrazin-2-yl)thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | 3-(Benzyloxy)-5-bromopyrazin-2-amine | HCID 10755162 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzoyl-3-(3-(benzyloxy)-5-bromopyrazin-2-yl)thiourea | HCID 86639654 | 66% |
Reaction Steps
Following the method of Example 1, Step B, benzoyl isothiocyanate (1.47 g, 8.99 mmol) and 3-(benzyloxy)-5-bromopyrazin-2-amine (2.29 g, 8.18 mmol) were reacted in THF (30 mL) to provide 1-benzoyl-3-(3-(benzyloxy)-5-bromopyrazin-2-yl)thiourea (2.38 g, 66%) as a yellow powder. 1H NMR (CDCl3) δ 8.15 (bs, 1H), 7.91 (d, 2H), 7.66 (t, 1H), 7.53-7.57 (m, 4H), 7.36-7.44 (m, 3H), 5.55 (s, 2H). Mass spectrum (apci) m/z=202 (100), 443 (45), 445 (43) (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933077B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-72511a554824423889cb1d0e835a87db |
| Source note | uspto-grants-2015_01 |