HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717553Generated: November 2, 2026
2-Amino-4-chloropyridine → HCID 178429763, compound
https://huagongshe.com/reaction/717553
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-4-chloropyridine | HCID 581866 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | HCID 71743410 | HCID 71743410 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178429763 | HCID 178429763 | — |
Reaction Steps
Potassium bis(trimethylsilyl)amide (1.0 M, 4.1 mL, 0.0041 mol) was added slowly for a period of 5 min to a solution of 4-chloro pyridin-2-amine (0.35 g, 0.00273 mol) in anhydrous tetrahydrofuran (30 mL) at 0° C. and stirred for 15 min at same temperature. Then 4-methyl-5-fluoronicotinonitrile (0.37 g, 0.00273 mol) in tetrahydrofuran (5 mL) was added. The reaction temperature was raised to RT and the reaction mixture was stirred it for 18 h. The reaction mixture was quenched with a saturated aqueous ammonium chloride solution (30 mL) and extracted with ethyl acetate (2×50 mL). The combined organic layers were dried over sodium sulphate and concentrated under vacuum to afford the crude product, which was purified by silica gel column chromatography to afford the title compounds. 1H NMR (400 MHz, CDCl3) δ 10.60 (bs, 1H), 8.53 (s, 1H), 8.43 (s, 1H), 8.25-8.24 (d, J=4 Hz, 1H), 7.25-7.24 (d, J=4 Hz, 1H), 7.02-7.00 (d, J=4 Hz, 1H), 2.48 (s, 3H), MS (M+1): 265.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193724B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-4715e5907f8149f5b0df38d63437e244 |
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| Source note | uspto-grants-2015_11 |
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