HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyclopropyl-6-methyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile → 3-(Aminomethyl)-4-cyclopropyl-6-methyl-2(1H)-pyridinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyclopropyl-6-methyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile | HCID 67124052 | — |
| Reactant | 3-(aminomethyl)-4-cyclohexyl-6-methyl-2(1H)-pyridinone | HCID 67124359 | — |
| Product | 3-(Aminomethyl)-4-cyclopropyl-6-methyl-2(1H)-pyridinone | HCID 67124208 | — |
Reaction Steps
The title compound was prepared in the same manner as described for 3-(aminomethyl)-4-cyclohexyl-6-methyl-2(1H)-pyridinone (Intermediate 3) using 4-cyclopropyl-6-methyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile (5 g, 28.7 mmol). Obtained: 0.50 g (10%). LCMS E-S (M+H)=179.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 11.76-11.78 (br s, 1H), 7.82-7.92 (br s, 3H), 5.61 (s, 1H), 3.94-3.99 (m, 2H), 2.11 (s, 3H), 1.98-2.05 (m, 1H), 0.95-1.01 (m, 2H), 0.74-0.79 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536179B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-2112b9d3d5134d578e5a4502bee417f6 |
| Source note | uspto-grants-2013_09 |