HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 2-amino-6-morpholino-3-nitroisonicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 2-Amino-6-morpholino-3-nitroisonicotinic acid | HCID 89647989 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-amino-6-morpholino-3-nitroisonicotinate | HCID 89648265 | 37.1% |
Reaction Steps
A mixture of 2-amino-6-morpholino-3-nitroisonicotinic acid (12.3 g, 45.9 mmol), HATU (19.2 g, 50.5 mmol), MeOH (14.7 g, 459 mmol) and Et3N (13.9 g, 137.7 mmol) in THF (300 mL) was stirred at room temperature for 16 h. The solvent was removed in vacuo and the residue was diluted with EA (500 mL). It was then washed with brine (500 mL×3). The organic layer was then concentrated in vacuo. The residue was then purified by chromatography on silica gel eluted with MeOH/DCM=1/100 to afford the crude product as a yellow solid (4.8 g, 37%); LC/MS: MS (ES+) m/e 283 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08906910B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-549ab2ed1806421dba7571cceb7d65f1 |
| Source note | uspto-grants-2014_12 |