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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426995Generated: October 30, 2026

Thionyl Chloride → 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbonyl chloride

https://huagongshe.com/reaction/426995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-Oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acidHCID 291530—
ReactantBistrimethylsilylacetamidHCID 11708267—
SolventDichloromethaneHCID 6344—
Product4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbonyl chlorideHCID 20544473—

Reaction Steps

In a similar manner to that of Example 1--1), 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbonyl chloride, which was prepared from 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acid (1.8 g) and thionyl chloride (36 ml), was treated with a solution of 7-(D-2-phenylglycinamido)-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid formate (2.5 g) and bis(trimethylsilyl)acetamide (4.0 g) in methylene chloride (50 ml). Thus obtained reaction mixture was worked up in a similar manner to that of Example 1-4) to give powder (650 mg) of 7-[D-2-(4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxamido)-2-phenylacetamide]-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid, mp 103° to 105° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04172198
Source datasetuspto-grants-1979_10
ORD IDord-5e5aaf4ab7184c74ad64c3b817474fa8
Source noteuspto-grants-1979_10