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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679627Generated: November 1, 2026

N-Methylpiperidine → 6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penam

https://huagongshe.com/reaction/1679627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylpiperidineHCID 12291—
ReactantSodium AzideHCID 33557—
ReactantPiperidine, 1-methyl-, hydrochlorideHCID 205378—
ReactantHCID 70604455HCID 70604455—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penamHCID 178431921—

Reaction Steps

A mixture of 6-triphenylmethylamino-2,2-dimethyl-3-cyanopenam (4.39 g. 0.01 mole), anhydrous ethanol-free chloroform (20 ml.), powdered sodium azide (650 mg., 0.01 mole) and dry N-methylpiperidine (2.98 g., 0.03 mole) is heated to 58°-60° C. (internal temperature). To the mixture is added with stirring 5 ml. of a solution of dry N-methylpiperidine hydrochloride (1.5 g., 0.011 mole) in ethanol-free chloroform (20 ml.) every 15 minutes over a period of one hour. The mixture is stirred and heated for 1.5 hours at 58°-60° C. following the additions of N-methylpiperidine and is then charged with finely powdered sodium azide (650 mg.) and N-methylpiperidine hydrochloride (1.5 g., 0.011 mole) in ethanol-free chloroform (20 ml.). The reaction mixture is heated for an additional hour and is then cooled to room temperature and diluted with water (150 ml.) and ethanol-free chloroform (250 ml.). The mixture is thoroughly shaken and the chloroform phase then separated and washed with successively with 1N HCl (1 × 250 ml.) and water (1 × 150 ml.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04081455
Source datasetuspto-grants-1978_03
ORD IDord-e4cb7aa56b6b483fbdda7c25c395f17d
Source noteuspto-grants-1978_03