HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Pivaloylamino)pyridine → N-(3-isobutyrylpyridin-2-yl)pivalamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Pivaloylamino)pyridine | HCID 1051519 | — |
| Reactant | N-Methoxy-N,2-dimethylpropanamide | HCID 10866371 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | N-(3-isobutyrylpyridin-2-yl)pivalamide | HCID 67083010 | 69.4% |
Reaction Steps
A solution of N-(pyridin-2-yl)pivalamide (3.20 g, 18.0 mmol), n-BuLi (15.00 mL, 2.1 eq.) and N-methoxy-N-methylisobutyramide (2.60 g, 1.1 eq) were reacted as outlined in Scheme 1 to give 3.10 g (69%) of N-(3-isobutyrylpyridin-2-yl)pivalamide. Spectroscopic data: 1H NMR (300 MHz, CDCl3) δ ppm 1.21 (d, J=7.03 Hz, 6 H) 1.35 (s, 9 H) 3.55 (dt, J=13.70, 6.78 Hz, 1 H) 7.08 (dd, J=7.91, 4.69 Hz, 1 H) 8.19 (dd, J=8.20, 2.05 Hz, 1 H) 8.63 (dd, J=4.83, 1.90 Hz, 1 H) 11.51 (br. s., 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08703797B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-301e98587cde49488ebe13f1a6dc7c3a |
| Source note | uspto-grants-2014_04 |