HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 178487790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 178487963 | HCID 178487963 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178487790 | HCID 178487790 | 60% |
Reaction Steps
Diethyl azodicarboxylate (455 μL, 2.90 mmol, 3.0 eq) is added at 0° C. to a stirred solution of {trans-4-[3-hydroxy-2-(3-hydroxy-6-methoxy-quinolin-4-ylmethyl)-propyl]-cyclohexyl}-carbamic acid tert-butyl ester (430 mg, 0.97 mmol, 1.0 eq) in tetrahydrofuran (100 mL), followed by triphenylphosphine (761 mg, 2.90 mmol, 3.0 eq). After 2 hours stirring at room temperature, solvent is removed and the crude is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate, 5:1, v/v) to afford [trans-4-(6-methoxy-3,4-dihydro-2H-1-oxa-9-aza-phenanthren-3-ylmethyl)-cyclohexyl]-carbamic acid tert-butyl ester as an off-white solid (247 mg, 60% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321788B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-a161a3c33b51449ea0d49d28e04f59ad |
| Source note | uspto-grants-2016_04 |