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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37876Generated: October 29, 2026

Triethylamine → HCID 25095423, compound

https://huagongshe.com/reaction/37876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(2-Methyl-allyl)-4-(4-amino-phenyl)-piperazineHCID 66851403—
ReactantOxo-(2-phenyl-5,6,7,8-tetrahydro-indolizin-3-yl)-acetyl chlorideHCID 86649692—
SolventDichloromethaneHCID 6344—
ProductHCID 25095423HCID 2509542321.1%

Reaction Steps

To an ice-cold solution of 4-[4-(2-methyl-allyl)-piperazin-1-yl]-phenylamine (prepared as described in Reference Example 89, 500 mg, 2.16 mmol) and triethylamine (0.6 mL, 4.32 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, 726 mg, 2.52 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-methyl-allyl)-piperazin-1-yl]-phenyl}-2-oxo-2-(2-phenyl-5,6,7,8-tetrahydro-indolizin-3-yl)-acetamide (220 mg, 21%) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524705B2
Source datasetuspto-grants-2013_09
ORD IDord-8d62af025a17413e989bdbfd447899f0
Source noteuspto-grants-2013_09