HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(5-methylpyridin-2-yl)-2-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Nitrobenzoyl chloride | HCID 11875 | — |
| Reactant | 2-Amino-5-methylpyridine | HCID 15348 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(5-methylpyridin-2-yl)-2-nitrobenzamide | HCID 840320 | 52.3% |
Reaction Steps
To a stirring solution of 2-amino-5-methylpyridine (3.1 g, 29 mmol) in dichloromethane (200 mL) was added pyridine (7.3 mL, 90 mmol) followed by 2-nitrobenzoyl chloride (5.7 g, 30 mmol). After 4 h, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate (500 mL) and water (250 mL). The organic phase was separated and washed with water, brine, dried (MgSO4) and filtered, and then concentrated in vacuo to a volume of about 100 mL (precipitate observed). The mixture was then sonicated and allowed to stand overnight then filtered. The collected solid was then washed with diethyl ether, filtered and dried under vacuum to give 3.9 g (52%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07160878B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-29acaf0089c14269849bb2a6e3953dde |
| Source note | uspto-grants-2007_01 |