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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-chloropyridineHCID 581866—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 71743410HCID 71743410—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178429763HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193724B2
Source datasetuspto-grants-2015_11
ORD IDord-4715e5907f8149f5b0df38d63437e244
Source noteuspto-grants-2015_11