HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842642Generated: October 26, 2026
Acryloyl chloride → N-(5-{[5-Chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl]amino}-4-methoxy-2-{methyl-[2-(4-methylpiperazin-1-yl)ethyl]amino}phenyl)prop-2-enamide
https://huagongshe.com/reaction/1842642
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | N4-(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)-5-methoxy-N1-methyl-N1-[2-(4-methylpiperazin-1-yl)ethyl]benzene-1,2,4-triamine | HCID 86677275 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(5-{[5-Chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl]amino}-4-methoxy-2-{methyl-[2-(4-methylpiperazin-1-yl)ethyl]amino}phenyl)prop-2-enamide | HCID 86677274 | 63.1% |
Reaction Steps
A solution of acryloyl chloride (0.028 mL, 0.35 mmol) in CH2Cl2 (1 mL) was added dropwise to a stirred mixture of N4-(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)-5-methoxy-N1-methyl-N1-[2-(4-methylpiperazin-1-yl)ethyl]benzene-1,2,4-triamine (Intermediate 107, 0.174 g, 0.33 mmol) in CH2Cl2 (2.5 mL) under N2. The mixture was then stirred at r.t. for 1 h and was then diluted with CH2Cl2 (25 mL). This solution was washed with sat. NaHCO3 (25 mL) and the aqueous wash solution was extracted with CH2Cl2 (20 mL). The combined organic solutions were dried (MgSO4) and concentrated in vacuo. Purification by FCC, eluting with 0-8% CH3OH in CH2Cl2 gave the title compound (0.12 g, 63%) as a beige foam; 1H NMR: (CDCl3) 2.31 (3H, s), 2.35-2.6 (10H, m), 2.67 (3H, s), 3.00 (2H, t), 3.88 (3H, s), 5.64-5.82 (1H, m), 6.31-6.50 (2H, m), 6.79 (1H, s), 6.91 (1H, t), 7.29 (1H, t), 7.48 (1H, s), 8.47 (1H, s), 8.54 (2H, t), 8.94 (1H, s), 9.15 (1H, s), 9.38 (1H, s); m/z: ES+ MH+ 576.59.
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-f7f67497c4f544cd8a90afd0b8f2d5a5 |
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| Source note | uspto-grants-2015_02 |
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