HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37877Generated: October 29, 2026
Triethylamine → HCID 25122028, compound
https://huagongshe.com/reaction/37877
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-[4-(2,2-Dimethyl-propyl)-piperazin-1-yl-]-phenylamine | HCID 24279197 | — |
| Reactant | Oxo-(2-phenyl-5,6,7,8-tetrahydro-indolizin-3-yl)-acetyl chloride | HCID 86649692 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25122028 | HCID 25122028 | 36.5% |
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
| 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-27038262d7744d498bc2c42bceb5bb6d |
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| Source note | uspto-grants-2013_09 |
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