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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371245Generated: October 30, 2026

Phosphorus oxychloride → Chloro-N,N-dimethylformiminium chloride

https://huagongshe.com/reaction/371245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantAcetamide, 2-(trimethylsilyl)-HCID 357676—
Reactant(2-Cyclohexen-1-yl)oxyamine hydrochlorideHCID 20274566—
Reactant2-(2-Cyclopenten-1-yl)oxyimino-2-[2-(2,2,2-trifluoroacetamido)thiazol-4-yl]acetic acidHCID 54095928—
ReactantN-[7-amino-3-cephem-3-ylmethyl]pyridinium-4-carboxylate dihydrochlorideHCID 70487017—
ReactantN-[7-[2-(2-cyclopenten-1-yl)oxyimino-2-{2-(2,2,2-trifluoroacetamido)thiazol-4-yl}acetamido]-3-cephem-3-ylmethyl]pyridinium-4-carboxylateHCID 131713029—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductChloro-N,N-dimethylformiminium chlorideHCID 77311—
ProductN-[7-{2-(2-cyclopenten-1-yl)oxyimino-2-(2-amino-thiazol-4-yl)acetamido}-3-cephem-3-ylmethyl]pyridinium-4-carboxylateHCID 131713027—

Reaction Conditions

Temperature40 °C

Reaction Steps

The solution of Vilsmeier reagent was prepared from dry N,N-dimethylformamide (0.48 g), phosphoryl chloride (1.0 g), ethyl acetate (4 ml) and tetrahydrofuran (15 ml) in a usual manner. To the solution was added 2-(2-cyclopenten-1-yl)oxyimino-2-[2-(2,2,2-trifluoroacetamido)thiazol-4-yl]acetic acid (syn isomer) (1.9 g) under ice cooling and the resulting solution was stirred for 30 minutes (Solution A). A mixture of N-[7-amino-3-cephem-3-ylmethyl]pyridinium-4-carboxylate dihydrochloride (2.0 g), trimethylsilylacetamide (5.7 g) and tetrahydrofuran (40 ml) was warmed to 40° C. and stirred to give a homogeneous solution, which was cooled to -25° C. and then thereto was added Solution A. The resulting mixture was stirred for 30 minutes around -10° C. To the reaction mixture containing N-[7-[2-(2-cyclopenten-1-yl)oxyimino-2-{2-(2,2,2-trifluoroacetamido)thiazol-4-yl}acetamido]-3-cephem-3-ylmethyl]pyridinium-4-carboxylate (syn isomer) were added ethyl acetate (50 ml) and water (100 ml). The ethyl acetate layer was separated and extracted with a saturated aqueous solution of sodium bicarbonate (50 ml). The extract and the remaining aqueous layer was combined, adjusted to pH 6.0 with 4N aqueous solution of sodium hydroxide and then thereto was added sodium acetate (7.5 g). The mixture was stirred for 41 hours at room temperature, adjusted to pH 2.0 with 10% hydrochloric acid, and then filtered. The filtrate was subjected to column chromatography (non-ion adsorption resin, Diaion HP20 prepared by Mitsubishi Chemical Industries) (60 ml) and the column was washed with water and then eluted with 10% isopropyl alcohol and 30% methanol. The eluates containing the object compound were collected, evaporated and lyophilized. The obtained powder was dried over phosphorus pentoxide under reduced pressure to give N-[7-{2-(2-cyclopenten-1-yl)oxyimino-2-(2-amino-thiazol-4-yl)acetamido}-3-cephem-3-ylmethyl]pyridinium-4-carboxylate (syn isomer) (0.3 g). mp. 171° to 180° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529802
Source datasetuspto-grants-1985_07
ORD IDord-f7118b5424a345ea83ed4b4bd8bbce99
Source noteuspto-grants-1985_07