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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413432Generated: November 1, 2026

Methanesulfonic Acid → HCID 13319610, compound

https://huagongshe.com/reaction/2413432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13319619HCID 13319619—
SolventAcetonitrileHCID 6342—
ProductHCID 13319610HCID 1331961098.9%

Reaction Conditions

Temperature23 °C

Reaction Steps

Methanesulphonic acid (0.3 cc) is added to a suspension of 2-benzhydryloxycarbonyl-7-t-butoxycarbonylamino-3-[2-(2-dimethylamino-ethylamino)-thiazol-5-yl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene (0.3 g) in acetonitrile (3 cc). The yellow solution obtained is stirred at 23° C. for 5 minutes and is poured onto a mixture of a saturated sodium bicarbonate solution (50 cc) and ethyl acetate (50 cc). The organic phase is dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure (20 mm Hg; 2.7 kPa). 7-Amino-2-benzhydryloxycarbonyl-3-[2-(2-dimethylamino-ethylamino)-thiazol-5-yl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene (0.25 g) is thus obtained in the form of a yellow froth.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04496560
Source datasetuspto-grants-1985_01
ORD IDord-d4711ea2fd134abdb04d4e3591272c69
Source noteuspto-grants-1985_01