Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370596Generated: October 28, 2026

p-Toluenesulfonic acid → HCID 13175153, compound

https://huagongshe.com/reaction/370596

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 13175939HCID 13175939—
SolventAcetonitrileHCID 6342—
ProductHCID 13175153HCID 1317515385.9%

Reaction Steps

3-(2-Acetamidothiazol-5-yl)-2-benzhydryloxycarbonyl-7-t-butoxycarbonylamino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene (4.6 g) is dissolved in acetonitrile (190 cc) at 35° C. and treated with a solution of p-toluenesulphonic acid (monohydrate) (2.9 g) in acetonitrile (20 cc) for 3 hours at 35° C., for 16 hours at 25° C. and then for a further 6 hours at 35° C. after the addition of p-toluenesulphonic acid (monohydrate) (0.95 g). The reaction mixture is partially concentrated under reduced pressure (30 mm Hg; 4 kPa) at 30° C. and then diluted with methylene chloride (200 cc) and a saturated solution of sodium bicarbonate (200 cc). The aqueous layer is extracted with methylene chloride (100 cc) and the combined organic solutions are washed with water (200 cc) and then dried and concentrated under reduced pressure (30 mm Hg; 4 kPa) at 30° C. The residue is dried under reduced pressure (10 mm Hg; 1.3 kPa) at 25° C. This gives crude 3-(2-acetamidothiazol-5-yl)-7-amino-2-benzhydryloxycarbonyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene (3.3 g) in the form of a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04526962
Source datasetuspto-grants-1985_07
ORD IDord-88ecc2b08b1d427caf42c126eef32736
Source noteuspto-grants-1985_07