HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178294Generated: October 29, 2026
Diisopropylethylamine → HCID 86663355, compound
https://huagongshe.com/reaction/2178294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile | HCID 2733849 | — |
| Reactant | HCID 66796681 | HCID 66796681 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 86663355 | HCID 86663355 | 86.2% |
Reaction Steps
A mixture of 2-methyl-1-[(3S)-pyrrolidin-3-yl]propan-1-amine (310 mg, 1.98 mmol), 2,6-dichloro-5-fluoro-pyridine-3-carbonitrile (378.7 mg, 1.98 mmol) and DIPEA (512.6 mg, 690.8 μL, 3.97 mmol) in NMP (3 mL) was heated at 130° C. for 20 minutes under microwave conditions. After this time, the reaction mixture was allowed to cool to ambient temperature and diluted with EtOAc, water and saturated aqueous NaHCO3. The organic layer was separated and washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The crude mixture was purified by column chromatography (ISCO Companion™, 40 g column, eluting with MeOH/DCM) to give the sub title compound as an oil (506.3 mg, 86% Yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067932B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-a301786b574c4974bf860dfe71262b07 |
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| Source note | uspto-grants-2015_06 |
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