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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361310Generated: October 25, 2026

Sodium amide → [[(6-Chloro-3-pyridinyl)amino]methylidene]-bisphosphonic acid tetraethylester

https://huagongshe.com/reaction/361310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium amideHCID 24533—
ReactantTriethyl phosphiteHCID 31215—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Amino-2-chloropyridineHCID 79305—
ReactantDiethyl (iodomethyl)phosphonateHCID 82616—
SolventCarbon TetrachlorideHCID 5943—
SolventTetrahydrofuranHCID 8028—
Product[[(6-Chloro-3-pyridinyl)amino]methylidene]-bisphosphonic acid tetraethylesterHCID 54442006—

Reaction Steps

6-Chloro-3-aminopyridine was alkylated with diethyl iodomethylphosphonate, sodium amide as base, with known methods. The obtained 6-chloro-3-pyridinylamino-methylphosphonic acid diethylester (0.5 mol) and N-bromosuccinimid (0.5 mol) in anhydrous carbontetrachloride is irradiated 2 hours with a 200 W lamp. The solid is filtered off, washed with carbontetrachloride and the solution is concentrated in vacuo. The obtained 6-chloro-3-pyridinylamino(bromomethyl)-phosphonic acid diethylester (0.1 mol) is warmed in tetrahydrofuran with triethylphosphite (0.1 mol) in 50° C. for 4 hours. The reaction mixture is concentrated in vacuo. The product is purified chromatographically (eluent dichloromethane: methanol 9:1). Yield 5.1 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866556
Source datasetuspto-grants-1999_02
ORD IDord-5fd55d8448eb42f3a163a04a6d76f5db
Source noteuspto-grants-1999_02