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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412471Generated: October 26, 2026

Acetic Acid → (R)-3-{4-[(4-tert-butylphenylamino)methyl]benzoylamino}-2-hydroxypropionic acid

https://huagongshe.com/reaction/412471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-Tert-ButylanilineHCID 69861—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(R)-3-(4-Formylbenzoylamino)-2-hydroxypropionic acidHCID 86586064—
SolventMethanolHCID 887—
SolventTrimethyl orthoformateHCID 9005—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(R)-3-{4-[(4-tert-butylphenylamino)methyl]benzoylamino}-2-hydroxypropionic acidHCID 69733516—

Reaction Steps

The above resin bound (R)-3-(4-formylbenzoylamino)-2-hydroxypropionic acid was treated with a 0.5 M solution of 4-tert-butylaniline (0.25 mmol) in a mixture of N-methyl-2-pyrrolidinone and trimethylorthoformate (1:1, 0.5 mL) and glacial acetic acid (50 μL) for 1 hour at 25° C. Sodium cyanoborohydride (250 μmol, 16 mg) dissolved in a mixture of N-methyl-2-pyrrolidinone and methanol (1:1, 0.25 mL) was added and the mixture was vortexed at 25° C. for 4 hours followed by filtration and washing with a mixture of N-methyl-2-pyrrolidinone and methanol (1:1, 2×1 mL) 3×1 mL N-methyl-2-pyrrolidinone (3×1 mL) and a mixture of 1,2-dichloropropane and diisopropylethylamine (7:1, 2×0.75 mL).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562807B2
Source datasetuspto-grants-2003_05
ORD IDord-71b30c3050734183ba963e75d25f19ae
Source noteuspto-grants-2003_05