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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109330Generated: November 1, 2026

Boron trifluoride → HCID 18646194, compound

https://huagongshe.com/reaction/1109330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantSodium HydroxideHCID 14798—
Reactant7-Aminocephalosporanic acidHCID 441328—
ReactantHCID 178429709HCID 178429709—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 18646194HCID 18646194—

Reaction Steps

A mixture of 2.80 g of 7-mercapto-5-methylpyrazolo[1,5-a]pyrimidine-3-carboxamide ammonium salt and 3.38 g of (7R)-7-aminocephalosporanic acid was treated with 25 ml of a 20 percent solution of boron trifluoride in acetonitrile and stirred at 20° for 40 minutes. The reaction mixture was treated with 30 ml of water and the pH was adjusted to 3.5 by means 28 percent aqueous sodium hydroxide solution. The precipitate thus formed was filtered off under suction and was chromatographed on OPTI-UP (C12) (ANTEC AG, CH-Bennwil) using water as the eluent. There was obtained (6R,7R)-7-amino-3-[[(3-carbamoyl-5-methylpyrazolo[1,5-a]-pyrimidin-7-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo-[4.2.0]oct-2-ene-2-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05319140
Source datasetuspto-grants-1994_06
ORD IDord-99fb95cf3fac4da8a120f366b48c7da1
Source noteuspto-grants-1994_06