HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37876Generated: October 29, 2026
Triethylamine → HCID 25095423, compound
https://huagongshe.com/reaction/37876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(2-Methyl-allyl)-4-(4-amino-phenyl)-piperazine | HCID 66851403 | — |
| Reactant | Oxo-(2-phenyl-5,6,7,8-tetrahydro-indolizin-3-yl)-acetyl chloride | HCID 86649692 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25095423 | HCID 25095423 | 21.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524705B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-8d62af025a17413e989bdbfd447899f0 |
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| Source note | uspto-grants-2013_09 |
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