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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720034Generated: October 26, 2026

Diisopropylethylamine → HCID 58737501, compound

https://huagongshe.com/reaction/720034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(p-Chlorophenyl)cyclobutanecarboxylic acidHCID 602761—
ReactantPyBroPHCID 2733179—
ReactantMethyl azetidine-3-carboxylate hydrochlorideHCID 21100040—
SolventDichloromethaneHCID 6344—
ProductHCID 58737501HCID 5873750170.6%

Reaction Steps

To a stirred solution of azetidine-3-carboxylic acid methyl ester hydrochloride (762 mg, 4.60 mmoles) and 1-(4-chloro-phenyl)-cyclobutane carboxylic acid (2.09 g, 9.90 mmoles) in anhydrous DCM (20 mL) was added di-isopropyl ethyl amine (4.6 mL, 26.4 mmoles) dropwise. After completion of addition solid PyBroP (4.63 g, 9.94 mmoles) was added to the stirring reaction mixture. The reaction mixture continued stirring at RT for 10 h and was quenched with water. The aqueous layer was extracted with EtOAc (3×20 mL). Combined organic layers were dried over Na2SO4 and concentrated to yield an oil. This crude material was purified using silica gel chromatography (9:1 hexanes:EtOAc-1:1 hexane:EtOAc) to yield the desired amide (1.0 g, 65%). 1H NMR (300 MHz, CDCl3): δ 7.38–7.29 (m, 4H), 4.16 (m, 2H), 3.88 (m, 1H), 3.72 (s, 3H), 3.31–1.63 (m, 8H). LRMS: M+309.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132551B2
Source datasetuspto-grants-2006_11
ORD IDord-63183ad97211417d99ce4ab82cde26db
Source noteuspto-grants-2006_11