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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192913Generated: October 29, 2026

Triethylamine → Tert-butyl 3-(2-ethoxy-2-oxoethyl)-3-(5-(phenylethynyl)furan-2-carboxamido)-azetidine-1-carboxylate

https://huagongshe.com/reaction/1192913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,5-Dioxopyrrolidin-1-yl 5-(phenylethynyl)furan-2-carboxylateHCID 57440810—
ReactantTert-butyl 3-amino-3-(2-ethoxy-2-oxoethyl)azetidine-1-carboxylateHCID 58109966—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 3-(2-ethoxy-2-oxoethyl)-3-(5-(phenylethynyl)furan-2-carboxamido)-azetidine-1-carboxylateHCID 6686534581%

Reaction Steps

A stirred solution of tert-butyl 3-amino-3-(2-ethoxy-2-oxoethyl)azetidine-1-carboxylate (130 mg, 0.503 mmol) in DMF (3 mL) was treated with NEt3 (0.19 mL, 1.37 mmol), and 2,5-dioxopyrrolidin-1-yl 5-(phenylethynyl)furan-2-carboxylate, prepared as described in Preparation 5 (141 mg, 0.457 mmol). The reaction was stirred overnight, at room temperature, then the solvent removed in vacuo and the crude product purified by column chromatography to obtain the title compound (168 mg, 81%). 1H NMR (400 MHz, CDCl3) δ 7.57 (m, 2H), 7.40 (m, 3H), 7.12 (s, 1H), 7.04 (s, 1H), 6.70 (s, 1H), 4.17 (m, 4H), 4.03 (d, 2H, J=9.6 Hz), 3.17 (s, 2H), 1.45 (s, 9H), 1.26 (t, 3H, J=7.2 Hz); MS ESI 453.2 [M+H]+, calcd for [C25H28N2O6+H]+ 453.51.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680282B2
Source datasetuspto-grants-2014_03
ORD IDord-5e23ef891c124963aa390eb1d192fc06
Source noteuspto-grants-2014_03