HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415412Generated: October 30, 2026
Diisopropylethylamine → HCID 178461870, compound
https://huagongshe.com/reaction/415412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (S)-1-(5-Fluoropyrimidin-2-yl)ethanamine hydrochloride | HCID 66624037 | — |
| Reactant | HCID 178506347 | HCID 178506347 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 178461870 | HCID 178461870 | 62% |
Reaction Steps
To a microwave vial was added (S)-1-(5-fluoropyrimidin-2-yl)ethanamine hydrochloride (Method 7, 81 mg, 0.46 mmol), 2,5-dichloro-N-[5-(2,2,2-trifluoroethoxy)-1H-pyrazol-3-yl]pyrimidin-4-amine (Method 40, 100 mg, 0.31 mmol), and DIEA (110 mg, 0.9 mmol). Anhydrous n-BuOH (2.5 mL) was added, and the vial was heated in microwave oven at 165° C. for 5 hours. The reaction mixture was concentrated. The resulting residue was separated by silica gel column to afford desired product (80 mg, 62%). LC-MS, 433 (M+1). 1H NMR δ 12.19 (s, 1H), 9.76 (s, 1H), 8.83 (s, 2H), 7.92-8.10 (m, 2H), 5.67 (s, 1H), 5.13 (s, 1H), 4.75 (m, 2H), 1.49 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088784B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-44a9842f25df486e9de12944bfd9da74 |
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| Source note | uspto-grants-2012_01 |
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