HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13839325, compound → HCID 14836042, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13839325 | HCID 13839325 | — |
| Reactant | HCID 14836041 | HCID 14836041 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14836042 | HCID 14836042 | 50% |
Reaction Steps
According to the procedure of O. M. Mitsunobu et al, Bull. Chem. Soc. Japan, 45, 3607 (1972), a solution of ethoxycarbonyl-t-butylcarbodiimide (0.436, 1.10 q) and N-[[2-fluoro-6-methoxy-5-(trifluoromethyl)-1-naphthalenyl]carbonyl]-N-methylglycine (0.838 g, 2.38 mmole) in anhydrous THF (13.5 mL) was heated to reflux under a dry nitrogen atmosphere for 10 hours. The reaction was cooled to room temperature and the organic solvent was removed. The solid was flash chromatographed (1:1 pertroleum ether:ethyl acetate, silica). The resultant foam was triturated with petroleum ether and dried to provide the title compound as a white solid (0.567 g, 50%), m.p. 130°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04962224 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-2b34fb07cdaf43a4a44f544f525817de |
| Source note | uspto-grants-1990_10 |