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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106115Generated: October 25, 2026

acetyl-DL-leucine → HCID 178474741, compound

https://huagongshe.com/reaction/1106115

Reaction equation

Participants

RoleNameHCIDCharge
Reactantacetyl-DL-leucineHCID 1995—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 178507442HCID 178507442—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 178474741HCID 17847474171.4%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of 13.0 g (75 mmol) of N-acetyl-DL-leucine, 10.5 ml (75 mmol) of triethylamine, and 150 ml of dichloromethane is stirred at -10° and 9.75 ml (75 mmol) of isobutyl chloroformate is added. The reaction mixture is stirred for 1/2 hour at -10° C. and a cold solution of 11.6 g (50 mmol) of 2-[4-aminophenyl)-4-hydroxy-5-pyrimidine carboxylic acid and 7.7 (55 mmol) of triethylamine in 200 ml of dimethylformamide is added. The mixture is stirred at 5° C. for 3 hrs and overnight at room temperature. The reaction mixture is evaporated and the residue treated with water. The pH is lowered to 2.5 with dilute hydrochloric acid and the solid filtered, washed with water, and dried to give 13.8 g of 2-[4-(N-acetyl-DL-leucylamino)phenyl]-4-hydroxy-5-pyrimidine carboxylic acid; mp 233°-235° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04311699
Source datasetuspto-grants-1982_01
ORD IDord-fceb47acaddf4b658971068ab3942754
Source noteuspto-grants-1982_01