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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402763Generated: October 31, 2026

Diisopropylethylamine → 1-Cyclobutyl-4-({1-[(6-methylpyridin-3-yl)carbonyl]azetidin-3-yl}carbonyl)piperazine

https://huagongshe.com/reaction/1402763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Methylnicotinoyl chlorideHCID 21890458—
Reactant1-(Azetidin-3-ylcarbonyl)-4-cyclobutylpiperazineHCID 66739315—
SolventDichloromethaneHCID 6344—
Product1-Cyclobutyl-4-({1-[(6-methylpyridin-3-yl)carbonyl]azetidin-3-yl}carbonyl)piperazineHCID 6673948619.3%

Reaction Steps

To a stirred solution of 1-(azetidin-3-ylcarbonyl)-4-cyclobutylpiperazine (60 mg, 0.27 mmol) in dichloromethane (1 mL) at 0° C., was added 6-methylpyridine-3-carbonyl chloride (31 mg, 0.32 mmol) and DIPEA (142 μL, 0.81 mmol). After 4 hours the reaction was quenched by addition of saturated aq. NaHCO3 (1 mL) and the aqueous extracted with dichloromethane (2×5 mL), dried (MgSO4), filtered, and concentrated at reduced pressure. Purification by silica FCC (eluting with 90:9:1 Et2O/MeOH/NH3) followed by capture and release on an SCX-2 cartridge (washing with MeOH and releasing with 7M NH3 in MeOH) gave the title compound (17.8 mg, 19%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912176B2
Source datasetuspto-grants-2014_12
ORD IDord-0527581ea75340cd89dd7708d751041c
Source noteuspto-grants-2014_12