Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388382Generated: November 2, 2026

Dimethylformamide dimethyl acetal → HCID 20239749, compound

https://huagongshe.com/reaction/1388382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 13281192HCID 13281192—
SolventMethanolHCID 887—
ProductHCID 20239749HCID 20239749—

Reaction Steps

A solution of the dihydrochloride salt of 4-(4,5-dihydro-1H-imidazol-2-yl)piperidine (0.99 g, 0.0044 M) in methanol (10 ml) which contained sodium methoxide (0.009 M) was stirred at room temperature for 10 minutes and dimethylformamide dimethylacetal (10 ml) was added and refluxed at 80° C. for 8 hrs. The excess of dimethylformamide dimethylacetal was removed to give 4-(4,5-dihydro-1H-imidazol-2-yl)-1-piperidinecarboxaldehyde dimethylacetal. To a mixtue of 6-aminopenicillanic acid (0.785 g, 0.0035 M) and diisopropyl ethylamine (0.412 ml) in dry chloroform was added the chloroform solution (30 ml) of the above piperidinecarboxaldehyde dimethyl acetal at 0° C. The reaction was stirred at 0° C. for 1 hr and at room temperature for 3 hrs. After this period, the solvent was removed in vacuo and the residue was dissolved in water (40 ml). The aqueous solution washed with ethylacetate was acidified to pH 3 with dil HCl and purified on Sephadex LH 20 columns to give [2S-(2alpha,5alpha,6beta)]-6-[[[4-(4,5-dihydro-1H-imidazol-2yl)-1-piperidinyl]methylene]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid hydrochloride (0.21 g, 11.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431653
Source datasetuspto-grants-1984_02
ORD IDord-3c18568edddd46e086c8c849fc39324a
Source noteuspto-grants-1984_02