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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614140Generated: October 30, 2026

Diazabicyclo[4.3.0]non-5-ene → 6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penam

https://huagongshe.com/reaction/614140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazabicyclo[4.3.0]non-5-eneHCID 21585024—
Reactant6-(Triphenylmethylamino)-2,2-dimethyl-3-(1-[2-methoxycarbonylethyl]tetrazol-5-yl)penamHCID 70605175—
SolventChloroformHCID 6212—
Product6(Triphenylmethylamino)-2,2-dimethyl-3-(5-tetrazolyl)penamHCID 17843192171%

Reaction Steps

To a stirred solution of 600 mg. of 6-(triphenylmethylamino)-2,2-dimethyl-3-(1-[2-methoxycarbonylethyl]tetrazol-5-yl)penam (containing ca 4.5% of methanol) in 1 ml. of chloroform, is added a solution of 375.2 mg. of diazabicyclo[4.3.0]non-5-ene in 0.5 ml. of chloroform. Stirring is continued for a further 3 hours, and then the solution is diluted with a further 2 ml. of chloroform. The latter solution is washed quickly with 5 ml. of 2N hydrochloric acid, and then a further 5 ml. of 2N hydrochloric are added. The resulting mixture is cooled to ca 0° C., and the solid which precipitates is filtered off, giving 323 mg. (71% yield) of the title compound. The NMR spectrum (DMSO-d6) of the product shows absorptions at 7.40 ppm(m, 15H), 5.30 ppm (s, 1H), 4.60 ppm (m, 2H), 1.58 ppm (s, 3H) and 0.78 ppm (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04143039
Source datasetuspto-grants-1979_03
ORD IDord-fe88065635ad4164b5723fef93e90eb2
Source noteuspto-grants-1979_03