HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396376Generated: October 31, 2026
6-Ethylpyridin-2-amine → HCID 86689738, compound
https://huagongshe.com/reaction/1396376
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Ethylpyridin-2-amine | HCID 89021 | — |
| Reactant | Ethyl 4,6-dichloropyridazine-3-carboxylate | HCID 53428795 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86689738 | HCID 86689738 | 35.5% |
Reaction Steps
4,6-Dichloro-pyridazine-3-carboxylic acid ethyl ester (500 mg, 2.26 mmol) and 6-ethylpyridin-2-amine 415 mg, 3.39 mmol) were dissolved in acetonitrile (7 mL), then heated at 140° C. for 3 d. The reaction mixture was cooled and concentrated in vacuo. Purification by chromatography (silica, 5 to 50% ethyl acetate in hexanes) gave 6-chloro-4-(6-ethyl-pyridin-2-ylamino)-pyridazine-3-carboxylic acid ethyl ester (246 mg, 35%) as a light brown solid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 10.68 (br. s., 1H) 9.30 (s, 1H) 7.61 (t, J=7.8 Hz, 1H) 6.91 (d, J=7.3 Hz, 1H) 6.77 (d, J=7.8 Hz, 1H) 4.57 (q, J=7.2 Hz, 2H) 2.86 (q, J=7.6 Hz, 2H) 1.52 (t, J=7.1 Hz, 3H) 1.38 (t, J=7.5 Hz, 3H); LCMS (EI/CI) m/z: 307 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901124B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-3e48a01bf9c942e3a1f06b567dd15964 |
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| Source note | uspto-grants-2014_12 |
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