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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106114Generated: October 25, 2026

N-Acetyl-DL-methionine → HCID 178503723, compound

https://huagongshe.com/reaction/1106114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetyl-DL-methionineHCID 6180—
ReactantDimethylacetamideHCID 31374—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 178507442HCID 178507442—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 178503723HCID 17850372357.1%

Reaction Steps

A suspension of 14.34 g (75 mmol) of N-acetyl-DL-methionine and 150 ml of dichloromethane is stirred at -15° and 10.5 ml (75 mmol) of triethylamine is added followed by 9.75 ml (75 mmol) of isobutyl chloroformate. After stirring for 20 minutes at -15° C., a solution of 11.6 g (50 mmol) of 2-(4-aminophenyl)-4-hydroxy-5-pyrimidine carboxylic acid in 200 ml of dimethylacetamide containing 7.7 ml (55 mmol) of triethylamine is added at -15° C. The mixture is stirred at 0° C. for 3 hrs and overnight at room temperature. The mixture is evaporated and the residue triturated with water. The aqueous suspension, after adjusting the pH to 2.5 with dilute HCl is filtered, washed with water, and dried to give 11.54 g of 2-[4-(N-acetyl-DL-methionylamino)phenyl]-4-hydroxy-5-pyrimidine carboxylic acid; mp 259° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04311699
Source datasetuspto-grants-1982_01
ORD IDord-05d69929a85042e98f25dfbd14c9cd8c
Source noteuspto-grants-1982_01