Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350964Generated: October 30, 2026

Triethylamine → HCID 86585855, compound

https://huagongshe.com/reaction/1350964

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-hydroxy4-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 C35H48N4O6 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 numberUS07214715B2
Source datasetuspto-grants-2007_05
ORD IDord-9b3b59605edc4b55b96911347bfcb071
Source noteuspto-grants-2007_05