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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353123Generated: November 2, 2026

Diisopropylethylamine → [1-(5-Cyclopentylmethyl-isoxazol-3-ylcarbamoyl)-butyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1353123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
Reactant(2S)-2-(((tert-butoxy)carbonyl)amino)pentanoic acidHCID 2733748—
Reactant5-(Cyclopentylmethyl)isoxazol-3-amineHCID 21102318—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product[1-(5-Cyclopentylmethyl-isoxazol-3-ylcarbamoyl)-butyl]-carbamic acid tert-butyl esterHCID 69470976—

Reaction Steps

(S)-2-tert-Butoxycarbonylamino-pentanoic acid (21.7 mmol) was dissolved in 100 mL of dichloromethane at rt under N2. Diisopropylethylamine (43.3 mmol) was added, followed by PyBOP (32.5 mmol). The reaction was stirred for 10 minutes at rt. The isoxazole R (21.7 mmol) was separately dissolved in 25 mL of dichloromethane and then added to the reaction solution. The resultant mixture was stirred at rt for 36-48 hours. The crude material was then diluted in 200 mL EtOAc and washed with two 100 mL portions of water, followed by 100 mL of brine. The organics were then dried over Na2SO4, filtered and concentrated under reduced pressure. The crude products were purified through flash chromatography on silica gel to give [1-(5-Cyclopentylmethyl-isoxazol-3-ylcarbamoyl)-butyl]-carbamic acid tert-butyl ester (14.0 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220865B2
Source datasetuspto-grants-2007_05
ORD IDord-f5129fe89b64433c95f4eecdd9689340
Source noteuspto-grants-2007_05