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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466232Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 19094385, compound

https://huagongshe.com/reaction/466232

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantBenzyl N-(5-hydroxypentyl)carbamateHCID 4072414—
ReactantHCID 76083370HCID 76083370—
SolventDimethylformamideHCID 6228—
ProductHCID 19094385HCID 19094385—

Reaction Steps

The compound of example 12(g) is prepared as follows: N-[2-(dimethylphosphonomethylamino)-3-(4-biphenylyl)-propionyl]-3-aminopropionic acid (700 mg; 1.61 mmol) in dimethyl formamide (DMF) (10 ml) is treated sequentially with N-benzyloxycarbonyl-5-aminopentanol (400 mg; 1.98 mmol) in DMF (2 ml), 1-hydroxybenzotriazole (HOBT) (265 mg; 1.96 mmol), 4-N,N-dimethylaminopyridine (DMAP) (239 mg; 1.96 mmol) and N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC) (553 mg; 3.22 mmol). The mixture is stirred for 20 hours, then partitioned between ethyl acetate (50 ml) and 1N HCl(30 ml). The organic layer is washed with a saturated solution of sodium bicarbonate (30 ml), then with brine (30 ml) before being dried over anhydrous sodium sulfate. After concentration under reduced pressure, the oily residue is purified by column chromatography on silica gel, eluting first with ethyl acetate, then with 5% methanol in methylene chloride to yield N-benzyloxycarbonyl-5-aminopentyl N-[2-(dimethylphosphonomethyl amino)-3-(4-biphenylyl)-propionyl]-3-aminopropionate as an oil; Rf(SiO2 ; MeOH/CH2Cl2):0.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155100
Source datasetuspto-grants-1992_10
ORD IDord-0e607a9af4414bfaa4ea3ad8b58b14fc
Source noteuspto-grants-1992_10