HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-methylpyridine → N-[(4-methylpyridin-2-yl)carbamothioyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-methylpyridine | HCID 1533 | — |
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[(4-methylpyridin-2-yl)carbamothioyl]benzamide | HCID 881443 | — |
Reaction Steps
A solution of 2-amino-4-methylpyridine (1.08 g, 10 mmol) and benzoyl isothiocyanate (1.63 g, 10 mmol) in acetone ( 15 mL) was stirred at RT for 1.5 h. The precipitate formed was filtered and washed with acetone to afford 1 -benzoyl-3-[4-methylpyridin-2-yl]-thiourea as a solid. This material was stirred with 2 N NaOH solution (15 mL) at 110° C. for 1 h, then cooled to RT, and the precipitate formed was washed with water and dried to provide (4-methylpyridin-2-yl)-thiourea (0.90 g, 53%). MS m/z 168 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084160B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-e587e61d27f4401dbb3291711c0d358c |
| Source note | uspto-grants-2006_08 |