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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609675Generated: November 1, 2026

Sodium Bicarbonate → HCID 131718946, compound

https://huagongshe.com/reaction/1609675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Chlorocarbonyl)-1,2-phenylene diacetateHCID 14096948—
ReactantHCID 131718127HCID 131718127—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 131718946HCID 13171894639.2%

Reaction Steps

The solution of 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-carboxymethoxyiminoacetamido]-3-(1-methyl-1-piperazinio)methyl-3-cephem-4-carboxylate (syn isomer) (540 mg) in acetone (5 ml) and water (5 ml) was adjusted to pH 7.0 with a saturated aqueous solution of sodium bicarbonate. To the mixture was added 3,4-diacetoxybenzoyl chloride (308 mg) at pH 6.5-7.0. The mixture was stirred for an hour and evaporated in vacuo to remove acetone. The residue was adjusted to pH 8.5 with a saturated aqueous solution of sodium bicarbonate and then stirred for 2 hours at room temperature. The mixture was adjusted to pH 3.5 with 3N hydrochloric acid and then filtered. The filtrate was subjected to column chromatography on Diaion HP-20 using 5% aqueous isopropyl alcohol as an eluent. The eluate was evaporated in vacuo to remove isopropyl alcohol and then lyophilized to give 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-carboxymethoxyiminoacetamido]-3-[1-methyl- 4-(3,4-dihydroxybenzoyl)- 1-piperazinio]methyl-3-cephem-4carboxylate (syn isomer) (265 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401734
Source datasetuspto-grants-1995_03
ORD IDord-04929ad1496d4399a252ba610f05d848
Source noteuspto-grants-1995_03