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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783224Generated: October 31, 2026

Triethylamine → HCID 86585855, compound

https://huagongshe.com/reaction/1783224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiethyl cyanophosphonateHCID 76257—
Reactant3-Cyano-5-[(dipropylamino)carbonyl]Benzoic AcidHCID 22593638—
ReactantHCID 58759815HCID 58759815—
SolventDichloromethaneHCID 6344—
ProductHCID 86585855HCID 86585855—

Reaction Steps

To a mixture of 3-cyano-5-[(dipropylamino)carbonyl]benzoic acid (IX/XXXII, PREPARATION 7, 0.086 g, 0.314 mmol) and tert-butyl (2R,3S)-3-amino-2-hydroxy-4-phenylbutyl(3-methoxybenzyl)carbamate (XXXV, EXAMPLE 584, 0.126 g, 0.314 mmol) in dichloromethane (0.3 mL) is added diethylcyanophosphonate (0.062 g, 0.330 mmol) and triethylamine (0.032 g, 0.316 mmol). The mixture is stirred at 20-25 degrees for 65 hours and then partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The organic phase is separated and dried over sodium sulfate and concentrated. The residue is chromatographed (silica gel, 20 mL; methanol/dichloromethane, 5/95) to give several mixed fractions, which are combined and rechromatographed (silica gel; acetone/hexane, 20/80) to give the title compound, MS (ESI+) for C38H48N4O6 m/z 657.6 (M+H)+=657.6; (M+Na)=679.5 and (M-C4H9O2)=557.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498436B2
Source datasetuspto-grants-2009_03
ORD IDord-3d482f4816a14eb0bd2a19510aac6c7a
Source noteuspto-grants-2009_03