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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456647Generated: November 2, 2026

Benzoyl chloride → ((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetic Acid Ethyl Ester

https://huagongshe.com/reaction/1456647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl N-benzyl-N-((tert-butoxycarbonyl)-L-valyl)glycinateHCID 23402347—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
Product((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetic Acid Ethyl EsterHCID 5393660398.9%

Reaction Steps

To a solution of compound 702 (3.45 g, 8.8 mmol) in EtOAc at 0° C. was bubbled in gaseous HCl until saturated. The reaction was warmed to rt and stirred for 3 hr. Nitrogen was bubbled through the reaction to remove excess HCl, followed by concentration in vacuo. The residue suspended in CH2Cl2 (50 mL), treated with DIEA (3.4 mL, 19.5 mmol) followed by benzoyl chloride (1.2 mL, 10.3 mmol) and the reaction allowed to stir overnight. The reaction was concentrated in vacuo and the residue taken up into EtOAc and H2O. The layers were separated and the organic phase washed with sat. aq. NaHCO3, sat. aq. KHSO4, brine, dried over MgSO4, filtered and concentrated in vacuo to provide 3.45 g of compound 703. ##STR82##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843904
Source datasetuspto-grants-1998_12
ORD IDord-a21eb8c73d2b4bda84cd88740187525e
Source noteuspto-grants-1998_12