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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371206Generated: October 30, 2026

Pyridine → 3-[[1,3-Dioxo-2-phenyl-3-(phenylmethoxy)propyl]amino]-3-methoxy-2-oxo-1-azetidinesulfonic acid, tetrabutylammonium salt

https://huagongshe.com/reaction/371206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantBenzyl (chlorocarbonyl)phenylacetateHCID 21289869—
Reactant3-Amino-3-methoxy-2-oxo-1-azetidinesulfonic acid tetrabutylammonium saltHCID 131714265—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product3-[[1,3-Dioxo-2-phenyl-3-(phenylmethoxy)propyl]amino]-3-methoxy-2-oxo-1-azetidinesulfonic acid, tetrabutylammonium saltHCID 13171426969.2%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Crude 3-amino-3-methoxy-2-oxo-1-azetidinesulfonic acid, tetrabutylammonium salt (431 mg, see Example 74), containing borax, is dissolved in 30 ml of dry acetonitrile. Dry pyridine (317 μl) is added and the solution stirred well at -10° C. under dry nitrogen. α-(Benzyloxycarbonyl)phenylacetyl chloride (568 mg) in 3 ml of dry acetonitrile is added dropwise. Thin layer chromatography indicates the reaction to be complete after 15 minutes. Potassium phosphate buffer (0.5M, pH 5.5, 17 ml) is added and most of the acetonitrile is removed in vacuo. The residue is diluted with water and extracted three times with equal volumes of methylene chloride. The extract is dried over anhydrous sodium sulfate and evaporated in vacuo to give 1.032 g of crude product, which is dissolved in 3 ml of methylene chloride and chromatographed on a silica column using methylene chloridemethanol to give 470 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529698
Source datasetuspto-grants-1985_07
ORD IDord-f58f009ab87a4a5da6f6881b33d50e5e
Source noteuspto-grants-1985_07