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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073811Generated: November 3, 2026

Hydrochloric Acid → HCID 23676283, compound

https://huagongshe.com/reaction/1073811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantMetam-sodiumHCID 5366415—
Reactant(6R-trans)-7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acidHCID 11031679—
Reactant(2Z)-2-[2-[(2-chloroacetyl)amino]-1,3-thiazol-4-yl]-2-methoxyiminoacetyl chloride;hydrochlorideHCID 12884125—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 23676283HCID 2367628355.1%

Reaction Steps

In 500 ml of a (1:1) mixture of water and THF was suspended 11.9 g of 7β-amino-3-hydroxymethyl-3-cephem-4-carboxylic acid, and 19.4 g of sodium hydrogencarbonate was added under ice-cooling and stirring. To the suspension was added 20.6 g of 2-(2-chloroacetamidothiazol-4-yl)-(Z)-2-methoxyiminoacetyl chloride hydrochloride, followed by stirring for 30 minutes. The reaction mixture was shaken with 100 ml of water and 150 ml of ethyl acetate. The aqueous layer was taken and adjusted to pH 7.0 with 1N-hydrochloric acid under ice-cooling and stirring. To the mixture was gradually added 12.0 g of sodium N-methyldithiocarbamate at room temperature under stirring to remove the amino group. After shaking with 200 ml of ethyl acetate, the aqueous layer was taken and concentrated to 50 ml under reduced pressure. The residue was subjected to a column chromatography on XAD-II (1.2l) eluting with water. The fractions containing the objective compound were collected, concentrated under reduced pressure, and then lyophilized to give 12.4 g of sodium 7β-[2-(2-aminothiazol-4-yl)-(Z)-2-methoxyiminoacetamido]-3-hydroxymethyl-3-cephem-4-carboxylate as pale yellow powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971963
Source datasetuspto-grants-1990_11
ORD IDord-30b3fb09926f40758fbf320b0728c48f
Source noteuspto-grants-1990_11