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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419723Generated: November 1, 2026

tert-Butanol → HCID 54344896, compound

https://huagongshe.com/reaction/1419723

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantHCID 54425150HCID 54425150—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 54344896HCID 54344896—

Reaction Steps

In 50 ml of dichloromethane were dissolved 1.7 g of (S,S)-4-[2-benzyloxycarbonylamino-3-(4-methoxyphenyl)propionyl]-3-(3-benzyloxycarbonylaminopropyl)-2-oxopiperazine-1-acetic acid produced in Reference Example 34, 2 ml of tert-butanol and 1.6 g of 4-dimethylaminopyridine. To the solution was then added 0.6 g of WSC, and the mixture was stirred for 24 hours at room temperature. Dichloromethane was distilled off, and the residue was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water and a saturated aqueous saline solution, which was then dried (Na2SO4), followed by concentration under reduced pressure. The concentrate was purified by means of a silica gel column chromatography (AcOEt), followed by crystallization from ether/hexane to afford 1.02 g of the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05888531
Source datasetuspto-grants-1999_03
ORD IDord-d47b4934dec24ea5a0dbe5ba5ba7336b
Source noteuspto-grants-1999_03