HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Isobutyl (3-methoxy-5-methylpyrazin-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 3-Methoxy-5-methyl-2-pyrazinamine | HCID 10701894 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Isobutyl (3-methoxy-5-methylpyrazin-2-yl)carbamate | HCID 10889995 | — |
Reaction Steps
Isobutylchloroformate (4.79 ml) was added to a stirred solution of 2-amino-3-methoxy-5-methylpyrazine (5 g) and pyridine (2.91 ml) in dichloromethane (10 ml) at ambient temperature. After 90 minutes the reaction mixture was diluted with dichloromethane (10 ml) and washed with 2M hydrochloric acid (3×20 ml), water (20 ml) and saturated sodium chloride solution (20 ml) and then dried (MgSO4). Volatile material was removed by evaporation to give a solid which was recrystallised from hexane to give isobutyl N-(3-methoxy-5-methylpyrazin-2-yl)carbamate (6.5 g); 1H NMR (CDCl3): 1.0 (d, 6 H), 2.0 (m, 1 H), 2.4 (s, 3 H), 4.0 (d, 2 H), 4.02 (s, 3 H), 7.3 (s, 1 H), 7.8 (s, 1 H); mass spectrum (positive chemical ionisation (+ve CI)): 240 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866568 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-5c3e0bcf16364091b5909209ee84f373 |
| Source note | uspto-grants-1999_02 |