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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744091Generated: October 30, 2026

Triethylamine → HCID 86594557, compound

https://huagongshe.com/reaction/1744091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPyBOPHCID 2724699—
ReactantAminoacetonitrile hydrochlorideHCID 11491918—
ReactantHCID 69152081HCID 69152081—
SolventDimethylformamideHCID 6228—
ProductHCID 86594557HCID 8659455755%

Reaction Steps

To a solution of N-(1-phenyl-1H-tetraazol-5-yl)-L-leucine (100 mg, 0.36 mmol), aminoacetonitrile hydrochloride (62 mg, 0.68 mmol) and PyBOP (230 mg, 0.44 mmol) in DMF (3 mL) was added triethylamine (0.2 mL, 1.4 mmol). The solution was stirred 36 h, then partitioned between ethyl acetate and pH 3 phosphate buffer. The organic phase was washed with brine and concentrated. Purification by flash chromatography (60% to 90% ethyl acetate/hexanes) gave 62 mg of N1-(cyanomethyl)-N2-(1-phenyl-1H-tetraazol-5-yl)-L-leucinamide. MS (+APCI): 313.9 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012075B2
Source datasetuspto-grants-2006_03
ORD IDord-cc03df82f4c5412db659575f1b09058c
Source noteuspto-grants-2006_03