HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446301Generated: October 26, 2026
Diisopropylethylamine → N-(4-(2-chloropyridin-3-yl)pyrimidin-2-yl)-4-(4-methylpiperazin-1-yl)benzamide
https://huagongshe.com/reaction/446301
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(4-methylpiperazin-1-yl)benzoyl Chloride | HCID 11630068 | — |
| Reactant | 4-(2-Chloropyridin-3-yl)pyrimidin-2-amine | HCID 53396335 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(4-(2-chloropyridin-3-yl)pyrimidin-2-yl)-4-(4-methylpiperazin-1-yl)benzamide | HCID 58588343 | — |
Reaction Steps
In a 48 mL sealed pressure vessel, added 4-(2-chloropyridin-3-yl)pyrimidin-2-amine (Step 1, 0.72 g, 3.5 mmol), 4-(4-methylpiperazin-1-yl)benzoyl chloride (1.0 g, 4.2 mmol), chloroform (5.0 mL), and N,N-diisopropylethylamine (0.73 mL, 4.2 mmol). The mixture was stirred at 50° C. for 17 hours, and concentrated to yield N-(4-(2-chloropyridin-3-yl)pyrimidin-2-yl)-4-(4-methylpiperazin-1-yl)benzamide as a light brown solid. MS (M+H)+=409; Calc'd 408.88 for C21H21ClN6O.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476434B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-c4ea6946b1de49629252793779d7f418 |
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| Source note | uspto-grants-2013_07 |
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