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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37877Generated: October 29, 2026

Triethylamine → HCID 25122028, compound

https://huagongshe.com/reaction/37877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-[4-(2,2-Dimethyl-propyl)-piperazin-1-yl-]-phenylamineHCID 24279197—
ReactantOxo-(2-phenyl-5,6,7,8-tetrahydro-indolizin-3-yl)-acetyl chlorideHCID 86649692—
SolventDichloromethaneHCID 6344—
ProductHCID 25122028HCID 2512202836.5%

Reaction Steps

To an ice-cold solution of 4-[4-(2,2-dimethyl-propyl)-piperazin-1-yl]-phenylamine (prepared as described in Reference Example 93, 300 mg, 1.21 mmol) and triethylamine (0.33 mL, 2.4 mmol) in dry DCM (12 mL) was added a solution of oxo-(2-phenyl-5,6,7,8-tetrahydro-indolizin-3-yl)-acetyl chloride (prepared as described in Reference Example 21, 407 mg, 1.41 mmol) in DCM (5 mL). The mixture was warmed to room temperature and stirred for 30 min then diluted with DCM, washed successively with water, sodium bicarbonate solution and brine, then dried over sodium sulfate. Concentration gave a residue which was purified by preparative TLC using ethyl acetate and hexane (3:7) as eluent to afford N-{4-[4-(2,2-dimethyl-propyl)-piperazin-1-yl]-phenyl}-2-oxo-2-(2-phenyl-5,6,7,8-tetrahydro-indolizin-3-yl)-acetamide (220 mg, 36%) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524705B2
Source datasetuspto-grants-2013_09
ORD IDord-27038262d7744d498bc2c42bceb5bb6d
Source noteuspto-grants-2013_09