Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706270Generated: October 29, 2026

Ethyl orthoformate → HCID 51030866, compound

https://huagongshe.com/reaction/706270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 57488457HCID 57488457—
ProductHCID 51030866HCID 51030866—

Reaction Steps

(4R,5S)-1-(3,4-diaminophenyl)-3-(4-methoxybenzyl)-5-(4-methoxyphenyl)-4-methylimidazolidin-2-one (0.105 g, 0.24 mmol) obtained from step F was dissolved in 3 mL triethyl orthoformate. The reaction was stirred for 30 minutes at reflux. After cooling the solvent was removed and the remains were dissolved in 8 mL trifluoroacetic acid. The reaction was stirred for 14 hours at ambient temperature. The TFA was removed under reduced pressure and the residue was re-dissolved in 20 mL of buffer (pH7) and three times extracted by means of 25 mL dichloromethane. The combined organic layers were washed with brine, dried over sodium sulfate, filtrated and the solvent was removed under reduced pressure. The final product was purified by FPLC using a chloroform-methanol gradient (0→10%). The product elutes at about 5% methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173885B2
Source datasetuspto-grants-2015_11
ORD IDord-e470237bd19f428ea490dd1eebd4b825
Source noteuspto-grants-2015_11