Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452057Generated: October 31, 2026

Ethyl orthoformate → HCID 51030866, compound

https://huagongshe.com/reaction/452057

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 numberUS08486940B2
Source datasetuspto-grants-2013_07
ORD IDord-0511659a19a140b5af9249eb711e934a
Source noteuspto-grants-2013_07