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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371539Generated: October 29, 2026

Diisopropylamine → HCID 21070243, compound

https://huagongshe.com/reaction/1371539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTriethylamineHCID 8471—
ReactantPyBroPHCID 2733179—
Reactant2-Tert-butoxycarbonylamino-3-(4-cyano-phenyl)-propionic acidHCID 4393346—
SolventDichloromethaneHCID 6344—
ProductHCID 21070243HCID 2107024331.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1 g of 2-(tert-butoxycarbonylamino)-3-(4-cyanophenyl)propionic acid and 0.540 g of diisopropylamine in 10 ml of DCM is cooled to 0° C., 0.960 ml of triethylamine is added, followed by addition of 1.76 g of bromotripyrrolidinophosphonium hexafluorophosphate, and the mixture is stirred for 2 hours and allowed to warm to RT. The reaction mixture is concentrated under vacuum, the residue is extracted with EtOAc, the organic phase is washed with water, with 5% KHSO4 solution, with water, with saturated NaHCO3 solution and with saturated NaCl solution and dried over Na2SO4, and the solvent is evaporated off under vacuum. The residue is chromatographed on silica gel, eluting with a heptane/EtOAc mixture (80/20; v/v). 0.4 g of the expected product is obtained; m.p.=172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157454B2
Source datasetuspto-grants-2007_01
ORD IDord-5980ba7a206745e889a10806ee087347
Source noteuspto-grants-2007_01