HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylbenzylamine → N-benzyl-N-methyl-2-(2-(phenylsulfonyl)ethylthio)nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2-[2-(Phenylsulfonyl)ethylthio]nicotinic acid | HCID 2821350 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-benzyl-N-methyl-2-(2-(phenylsulfonyl)ethylthio)nicotinamide | HCID 25221517 | 46.8% |
Reaction Steps
132 mg (0.81 mmol) of CDI were added to a solution of 250 mg (0.77 mmol) of 2-(2-(phenylsulfonyl)ethylthio)nicotinic acid in DCM (6 ml), and the mixture was stirred for 1 hour at RT. A solution of 93 mg (0.77 mmol) of N-benzyl-N-methylamine in DCM (6 ml) was then added, and stirring was continued for a further 16 h at RT. The reaction solution was then washed in each case three times with sat. aq. ammonium chloride solution and saturated aqueous NaHCO3 solution. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. CC with the residue (DCM→DCM/MeOH 99.5:0.5) yielded 152 mg (0.36 mmol, 46%) of N-benzyl-N-methyl-2-(2-(phenylsulfonyl)ethylthio)nicotinamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084470B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-b3877c58101e464f880a334d7caee8b1 |
| Source note | uspto-grants-2011_12 |