HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730757Generated: October 25, 2026
Diisopropylethylamine → HCID 178461513, compound
https://huagongshe.com/reaction/730757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloro-3-(trifluoromethyl)pyridine | HCID 589833 | — |
| Reactant | HCID 178461512 | HCID 178461512 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178461513 | HCID 178461513 | — |
Reaction Steps
A mixture of the piperazine from step (a) above (80 mg, 0.25 mmol), 2-chloro-3-trifluoromethyl-pyridine (54 mg, 0.3 mmol, Aldrich) and NAN-diisopropylethylamine (0.5 mL, 2.9 mmol, Aldrich) was heated in a microwave synthesizer for 120 min at 250° C. Water (10 mL) was added and the mixture was extracted with EtOAc (2×20 mL). The combined organic phases were washed with brine (10 mL), dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by silica gel chromatography, eluting with 35% EtOAc/hexane to give the title compound as a white amorphous solid. MS (ESI, pos. ion) m/z: 464 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582761B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-82cc65b4061249eca784c836b58739ad |
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| Source note | uspto-grants-2009_09 |
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