Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982363Generated: November 1, 2026

Sodium Hydroxide → (3S)-3-[[[2-(formylamino)-4-thiazolyl]acetyl]amino]-4-methyl-2-oxo-1-azetidinesulfonic acid

https://huagongshe.com/reaction/1982363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Thiazoleacetic acid, 2-(formylamino)-HCID 11286886—
Reactant(3S)-3-amino-4-methyl-2-oxo-1-azetidinesulfonic acidHCID 57095442—
Product(3S)-3-[[[2-(formylamino)-4-thiazolyl]acetyl]amino]-4-methyl-2-oxo-1-azetidinesulfonic acidHCID 57200001—

Reaction Steps

100 mg. of a Escherichia coli acylase that is bound in a polyacrylamide matrix (Boehringer Mannheim) is mixed with an aqueous solution containing 4 mg. of 2-(formylamino)-4-thiazoleacetic acid and an aqueous solution containing 2 mg. of (3S)-3-amino-4-methyl-2-oxo-1-azetidinesulfonic acid, inner salt in a total volume of 2 ml. The pH of the reaction mixture is adjusted to pH 4.5 by the addition of 50 mmolar sodium hydroxide. The reaction mixture is incubated at 30° C. with shaking (60 rpm) for up to 20 hours. The desired product can then be separated from the reaction mixture by thin layer chromatography using a silica gel 60 F254 plate and developing in a solvent consisting of acetonitrile, ethyl acetate, acetic acid, and water (4:4:1:1) followed by elution with water to give (3S)-3-[[[2-(formylamino)-4-thiazolyl]acetyl]amino]-4-methyl-2-oxo-1-azetidinesulfonic acid, zwitterion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596777
Source datasetuspto-grants-1986_06
ORD IDord-e701070d876943f79be34d059d844e0b
Source noteuspto-grants-1986_06