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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482838Generated: October 30, 2026

HCID 23706035, compound → HCID 131714535, compound

https://huagongshe.com/reaction/482838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23706035HCID 23706035—
SolventPropan-2-one--water (1/1)HCID 18366337—
ProductHCID 131714535HCID 131714535—

Reaction Steps

1.62 g (6.20 mmol) of (3S,4S)-3-amino-4-carbamoyloxymethyl-2-oxo-1-azetidinesulphonic acid sodium salt are dissolved in 180 ml of acetone/water (2:1) and treated with 3.27 g (6.83 mmol) of (Z)-2-(2-amino-4-thiazolyl)-2-[[1-(t-butoxycarbonyl)-1-methylethoxy]imino]-acetic acid 2-benzthiazolyl thioester. The mixture is stirred at room temperature for 12 hours. A further 60 mg (0.12 mmol) of the aforementioned thioester are added thereto and the stirring is continued for a further 3 hours. Acetone is removed under reduced pressure and 50 ml of water are added thereto. The crystals obtained are filtered off and washed with a small amount of water. The mother liquor is partially evaporated (37°, 15 mmHg) and the residue is chromatographed (MCI gel, H2O). After lyophilization, there are obtained 2.28 g (77%) of (3S,4S)-3-[2-amino-4-thiazolyl)-2-(Z)-[[1-(t-butyoxycarbonyl)-1-methylethoxy]imino]acetamido]-4-carbamoyloxymethyl-2-oxo-1-azetidinesulphonic acid sodium salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04576751
Source datasetuspto-grants-1986_03
ORD IDord-3a85d94841b445c5897b65610445855d
Source noteuspto-grants-1986_03