HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450376Generated: October 30, 2026
Diisopropylethylamine → HCID 178466925, compound
https://huagongshe.com/reaction/450376
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (S)-1-(5-Fluoropyrimidin-2-yl)ethanamine hydrochloride | HCID 66624037 | — |
| Reactant | 6-Chloro-N-(5-ethoxy-1H-pyrazol-3-yl)-3-nitropyridin-2-amine | HCID 178466919 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178466925 | HCID 178466925 | 84.6% |
Reaction Steps
A mixture of 6-chloro-N-(5-ethoxy-1H-pyrazol-3-yl)-3-nitropyridin-2-amine (Intermediate 26, 0.35 g) and [(1S)-1-(5-fluoropyrimidin-2-yl)ethyl]amine hydrochloride (Intermediate 15, 0.20 g) in n-BuOH (5 mL) with diisopropylethylamine (1 mL) was stirred at 70° C. for 4 hours. The resulting mixture was diluted with ethyl acetate (20 mL), and washed with brine (10 mL×3). The organic layer was dried and concentrated. The resulting residue was separated by silica gel column (Hexane/Ethyl acetate) to yield 0.37 g of the title compound. MS (electrospray): 389 (M+1) for C16H17FN8O3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486966B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-c06c3fd86be445e0b167a66e9bff7573 |
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| Source note | uspto-grants-2013_07 |
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