HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842722Generated: November 2, 2026
1-Methylpiperazine → HCID 71240767, compound
https://huagongshe.com/reaction/1842722
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 5-chloro-N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amine | HCID 71239348 | — |
| Solvent | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Product | HCID 71240767 | HCID 71240767 | 100% |
Reaction Steps
1-Methylpiperazine (0.267 mL, 2.41 mmol) was added to a suspension of 5-chloro-N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amine (Intermediate 20, 500 mg, 1.21 mmol) in 2,2,2-trifluoroethanol (6 mL). The mixture was heated in a microwave at 140° C. for 1 h. The mixture was then loaded onto a SCX column, and the column was washed with CH3OH. The column was then eluted with 2M methanolic ammonia and appropriate fractions were combined and concentrated in vacuo. Further purification by FCC, eluting with 0-10% CH3OH in CH2Cl2 gave the title compound (596 mg, 100%), as an orange foam; 1H NMR: (CDCl3) 2.37 (3H, s), 2.57-2.68 (4H, m), 3.08-3.14 (4H, m), 4.00 (3H, s), 6.64 (1H, s), 6.98 (1H, t), 7.34-7.43 (1H, m), 7.53 (1H, s), 8.41 (1H, s), 8.49 (1H, d), 8.53-8.6 (1H, m), 8.93 (1H, s), 9.04 (1H, s); m/z: ES+ MH+ 495.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946235B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-4defc220744d41e3ac48365b8151debf |
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| Source note | uspto-grants-2015_02 |
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