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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744116Generated: November 1, 2026

Triethylamine → N2-(4-bromo-1-methyl-1H-pyrazol-3-yl)-N1-(cyanomethyl)leucinamide

https://huagongshe.com/reaction/1744116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantPyBOPHCID 2724699—
ReactantAminoacetonitrile hydrochlorideHCID 11491918—
ReactantN-(4-bromo-1-methyl-1H-pyrazol-3-yl)leucineHCID 69151592—
SolventDimethylformamideHCID 6228—
ProductN2-(4-bromo-1-methyl-1H-pyrazol-3-yl)-N1-(cyanomethyl)leucinamideHCID 86594568—

Reaction Steps

To N-(4-bromo-1-methyl-1H-pyrazol-3-yl)leucine (366 mg, 1.26 mmol), PyBOP (725 mg, 1.39 mmol), aminoacetonitrile hydrochloride (257 mg, 2.78 mmol) in dry DMF (15 mL) under dry nitrogen was added triethylamine (0.62 mL, 4.45 mmol) dropwise and the reaction stirred for 2½ hours. Aqueous sat. NaHCO3 was added and the product extracted with Et2O (2×), dried over Na2SO4, concentrated in vacuo and purified by flash chromatography over silica gel (EtOAc/Hex, 6/4) to afford N2-(4-bromo-1-methyl-1H-pyrazol-3-yl)-N1-(cyanomethyl)leucinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012075B2
Source datasetuspto-grants-2006_03
ORD IDord-ca4d055fd75b417dac0ba279b0c59371
Source noteuspto-grants-2006_03