HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Methyl 4-((tert-butoxycarbonyl)amino)nicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acid | HCID 22172623 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-((tert-butoxycarbonyl)amino)nicotinate | HCID 23438729 | 81% |
Reaction Steps
To a stirring suspension of 4-(Boc-amino)pyridine-3-carboxylic acid (1.04 g, 4.37 mmol) in methanol (3.5 mL) was added a 2 M solution of (trimethylsilyl)diazomethane in hexanes (3.5 mL, 7 mmol). After 15 min, acetic acid was added and the solvents were removed in vacuo. The residue was chromatographed over silica gel, eluting with a step gradient of 20% ethyl acetate in hexanes through 70% ethyl acetate in hexanes. The product containing fractions were combined and concentrated in vacuo to give the title compound (0.894 g, 81%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07511066B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-5347db7719614c68834cfe16e6710679 |
| Source note | uspto-grants-2009_03 |