HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432562Generated: November 3, 2026
N-[4-(1-Ethyl-propyl)-6-methyl-pyridazin-3-yl]-2,2-dimethyl-propionamide → 6-Methyl-4-(pentan-3-YL)pyridazin-3-amine
https://huagongshe.com/reaction/1432562
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-[4-(1-Ethyl-propyl)-6-methyl-pyridazin-3-yl]-2,2-dimethyl-propionamide | HCID 68842351 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 6-Methyl-4-(pentan-3-YL)pyridazin-3-amine | HCID 53421610 | 82.2% |
Reaction Steps
N-[4-(1-Ethyl-propyl)-6-methyl-pyridazin-3-yl]-2,2-dimethyl-propionamide (12.0 g, 45 mmol) is dissolved in 60 mL of concentrated hydrochloric acid. The reaction mixture is heated to 95° C. in a sealed flask for 2 hours. The reaction is worked up by pouring over ice and extracting with ethyl acetate three times. The organic layer is discarded, and the pH of the aqueous layer is adjusted using 2 N sodium hydroxide. The basic solution is extracted with ethyl acetate five times. The organic extracts are combined, dried over magnesium sulfate, filtered, and evaporated to obtain 6.68 g (37 mmol, 81%) of the title compound as a brownish oil. 1H-NMR (DMSO-d6), δ 6.95 (s, 1H); 5.89 (s, br, 2H); 2.52-2.56 (m, 1H); 2.34 (s, 3H); 1.44-1.58 (m, 4H); 0.72 (t, J=7.04 Hz, 6H) ppm. MS/ES+=180 (100%, M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612067B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-bb47aa62f2e84ee7b7abae4b0532ad2c |
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| Source note | uspto-grants-2009_11 |
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