HuagongsheHuagongshe Chemistry Print Report · For research reference only
P,P-Diphenylphosphinic azide → HCID 22136236, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Methyl isocyanoacetate | HCID 547815 | — |
| Reactant | Potassium carbonate sesquihydrate | HCID 2734018 | — |
| Reactant | HCID 70699990 | HCID 70699990 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22136236 | HCID 22136236 | — |
Reaction Steps
To a cold (0° C.) mixture of Boc 3-carboxymethyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (3.893 g, 0.010 mol), and potassium carbonate sesquihydrate (6.606 g, 0.040 mol) in DMF (20 mL) was added diphenylphosphoryl azide (3.03 mL, 14.0 mmol) and methyl isocyanoacetate (1.9 mL, 20.9 mmol). The reaction mixture was stirred for 1 day at room temperature. The reaction was then diluted with aq NaCl and extracted with CHCl3 (150 mL). The organic solution was dried over Na2SO4, filtered and concentrated to a brown oil. The crude product was purified by flash chromatography twice (2% MeOH in CHCl3) to yield 3-(4-methoxycarbonyloxazol-5-ylmethyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylic acid-t-butyl ester as a tacky solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053101B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-6839ed8fe17e44c98fdd56fccff3388c |
| Source note | uspto-grants-2006_05 |