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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100307Generated: October 31, 2026

1-Propanesulfonyl chloride → 1-(Propylsulfonyl)-3-pyridin-2-ylazetidine-3-carbonitrile

https://huagongshe.com/reaction/2100307

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Propanesulfonyl chlorideHCID 66279—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Pyridin-2-ylazetidine-3-carbonitrile hydrochlorideHCID 68827153—
SolventDichloromethaneHCID 6344—
Product1-(Propylsulfonyl)-3-pyridin-2-ylazetidine-3-carbonitrileHCID 57798311—

Reaction Steps

A suspension of 3-pyridin-2-ylazetidine-3-carbonitrile hydrochloride (365 mg, 1.9 mmol) in CH2Cl2 (10 mL) at 0° C. was treated with i-Pr2NEt (1.1 mL, 6.3 mmol) and n-PrSO2Cl (0.35 mL, 3.1 mmol) dropwise. After 4 h, the reaction was quenched with the addition of 2 M aqueous NaOH (10 mL) and stirred 72 h before being extracted with CH2Cl2 (3×20 mL). The combined organic extracts were dried (Na2SO4) and concentrated under reduced pressure to afford 1-(propylsulfonyl)-3-pyridin-2-ylazetidine-3-carbonitrile (II-1) as an orange oil. Analytical LCMS: single peak (214 nm), 2.664 min. This material was used in subsequent reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572792B2
Source datasetuspto-grants-2009_08
ORD IDord-85be5606e24a4953b3d6be03293ed9a8
Source noteuspto-grants-2009_08