HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → Benzyl {3-[({5-[(tert-butoxycarbonyl)amino]pyridin-2-yl}carbonyl)(methyl)amino]propyl}methylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diphenylphosphate azide | HCID 21964642 | — |
| Reactant | 6-[(3-{[(Benzyloxy)carbonyl](methyl)amino}propyl)(methyl)carbamoyl]pyridine-3-carboxylic acid | HCID 66671547 | — |
| Product | Benzyl {3-[({5-[(tert-butoxycarbonyl)amino]pyridin-2-yl}carbonyl)(methyl)amino]propyl}methylcarbamate | HCID 66671652 | 64% |
Reaction Steps
The compound (449 mg, 1.16 mmol) obtained in Example 5b was dissolved in tert-butanol (6 mL), triethylamine (1.78 mL, 1.28 mmol) and diphenylphosphate azide (0.251 mL, 1.16 mmol) were added, and the mixture was stirred with heating to reflux for 3 hours. The solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:2→0:100, v/v) to give the title compound (339 mg; yield, 64%) as a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476253B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-1dcf2f0017974b1b8cfd47872842f1cf |
| Source note | uspto-grants-2013_07 |