HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → N-methyl-6-morpholin-4-yl-4-o-tolyl-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-chloro-N-methyl-4-o-tolyl-nicotinamide | HCID 12167312 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-methyl-6-morpholin-4-yl-4-o-tolyl-nicotinamide | HCID 22479279 | 92.9% |
Reaction Steps
A mixture of 1.00 g (3.84 mmol) 6-chloro-N-methyl-4-o-tolyl-nicotinamide, 0.37 ml (4.22 mmol) morpholine, 2.0 ml (12 mmol) N-ethyldiisopropylamine and a catalytic amount of 4-(N,N-dimethylamino)-pyridine was heated at 100° C. over night. After cooling to room temperature the mixture was dissolved in ethyl acetate and washed with two portions of water. The combined aqueous layers were extracted with 3 portions of dichloromethane. Drying with sodium sulfate and concentration gave 1.23 g of the crude product. Flash column chromatography afforded 1.11 g (92.9%) of the title compound as an off-white solid. M.p. 156-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06806370B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-28ff28548c524cf7ad8f5f4cf72e3ff7 |
| Source note | uspto-grants-2004_10 |