HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium amide → [[(6-Chloro-3-pyridinyl)amino]methylidene]-bisphosphonic acid tetraethylester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Amino-2-chloropyridine | HCID 79305 | — |
| Reactant | Diethyl (iodomethyl)phosphonate | HCID 82616 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [[(6-Chloro-3-pyridinyl)amino]methylidene]-bisphosphonic acid tetraethylester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866556 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-5fd55d8448eb42f3a163a04a6d76f5db |
| Source note | uspto-grants-1999_02 |