HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802256Generated: October 30, 2026
Diisopropylethylamine → HCID 86666020, compound
https://huagongshe.com/reaction/1802256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,7-Dibromo[1,2,4]triazolo[1,5-a]pyridine | HCID 67774274 | — |
| Reactant | (2-Fluoroethyl)(methyl)amine hydrochloride | HCID 85799809 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86666020 | HCID 86666020 | 34.5% |
Reaction Steps
To the solution of 2,7-dibromo-[1,2,4]triazolo[1,5-a]pyridine (5 g, 18.05 mmol) and (2-fluoro-ethyl)-methyl-amine hydrochloride (20 g, 180.5 mmol) in ethanol (30 ml) was added di-isopropylethylamine (47 ml, 270.75 mmol) and the reaction mixture was heated at 130° C. in a sealed tube for 84 hours. The reaction mixture was concentrated under reduced pressure, the resulting residue was diluted with dichloromethane (100 ml). The organic layer was washed with water (2×75 ml), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude material was purified by column chromatography over silicagel using 0.5% methanol/dichloromethane as eluent affording (7-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-(2-fluoro-ethyl)-methyl-amine (1.7 g, 34.5%) as an off white solid. MS: m/z=275.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349824B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-bfb48cd994424fccbde0b66bcaacd411 |
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| Source note | uspto-grants-2013_01 |
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