HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241874Generated: October 26, 2026
Diisopropylethylamine → (R)-6-(5-Methylpyridin-2-yl)-N-(1-(6-(trifluoromethyl)pyridin-3-yl)ethyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine
https://huagongshe.com/reaction/241874
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Chloro-5,6,7,8-tetrahydro-6-(5-methylpyridin-2-yl)pyrido[4,3-d]pyrimidine | HCID 59346457 | — |
| Reactant | (R)-1-(6-(Trifluoromethyl)pyridin-3-yl)ethan-1-amine dihydrochloride | HCID 66872458 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (R)-6-(5-Methylpyridin-2-yl)-N-(1-(6-(trifluoromethyl)pyridin-3-yl)ethyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine | HCID 25033574 | — |
Reaction Steps
To a stirred solution of (R)-1-(6-(trifluoromethyl)pyridin-3-yl)ethanamine dihydrochloride (44 mg, 0.17 mmol) and N,N-diisopropylethylamine (73 μL, 0.42 mmol) in acetonitrile (1.1 mL) was added 4-chloro-5,6,7,8-tetrahydro-6-(5-methylpyridin-2-yl)pyrido[4,3-d]pyrimidine (30 mg, 0.1 mmol). The reaction was capped and heated in the microwave for 10 hours at 180° C. The reaction mixture was quenched with excess water and allowed to stir for 10-15 minutes. The precipitated product was filtered, washed with water and dried in vacuum oven to obtain the title compound as a light tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653091B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-e6359e973d454fa69a0de36c76424e3a |
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| Source note | uspto-grants-2014_02 |
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