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8-(4-BROMOBENZOYL)-7-ETHOXYCARBONYL-7-HYDROXY-6-OXO-1,2,3,4,6,7-HEXAHYDROPYRROLO-[1,2-A]-PYRIMIDINE

Compound with spectra: 1 NMR, and 1 MS (GC)

8-(4-BROMOBENZOYL)-7-ETHOXYCARBONYL-7-HYDROXY-6-OXO-1,2,3,4,6,7-HEXAHYDROPYRROLO-[1,2-A]-PYRIMIDINE
SpectraBase Compound ID FjwB77I9sTh
InChI InChI=1S/C17H17BrN2O5/c1-2-25-16(23)17(24)12(13(21)10-4-6-11(18)7-5-10)14-19-8-3-9-20(14)15(17)22/h4-7,19,24H,2-3,8-9H2,1H3
InChIKey ORINFPATHOMKIP-UHFFFAOYSA-N
Mol Weight 409.24 g/mol
Molecular Formula C17H17BrN2O5
Exact Mass 408.032085 g/mol

View Spectrum of 8-(4-BROMOBENZOYL)-7-ETHOXYCARBONYL-7-HYDROXY-6-OXO-1,2,3,4,6,7-HEXAHYDROPYRROLO-[1,2-A]-PYRIMIDINE

MS (GC) Spectrum
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Source of Spectrum KC-0-325-10

View Spectrum of 8-(4-BROMOBENZOYL)-7-ETHOXYCARBONYL-7-HYDROXY-6-OXO-1,2,3,4,6,7-HEXAHYDROPYRROLO-[1,2-A]-PYRIMIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
  • 8-(4-bromobenzoyl)-7-hydroxy-6-keto-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrimidine-7-carboxylic acid ethyl ester
8-(4-CHLOROBENZOYL)-7-ETHOXYCARBONYL-7-HYDROXY-6-OXO-1,2,3,4,6,7-HEXAHYDROPYRROLO-[1,2-A]-PYRIMIDINE
7-ETHOXYCARBONYL-7-HYDROXY-8-(4-METHOXYBENZOYL)-6-OXO-1,2,3,4,6,7-HEXAHYDROPYRROLO-[1,2-A]-PYRIMIDINE
8-BENZOYL-7-ETHOXYCARBONYL-7-HYDROXY-6-OXO-1,2,3,4,6,7-HEXAHYDROPYRROLO-[1,2-A]-PYRIMIDINE
7-(4-BROMOBENZOYL)-6-ETHOXYCARBONYL-6-HYDROXY-5-OXO-2,3,5,6-TETRAHYDRO-1H-PYRROLO-[1,2-A]-IMIDAZOLE
7-(4-CHLOROBENZOYL)-6-ETHOXYCARBONYL-6-HYDROXY-5-OXO-2,3,5,6-TETRAHYDRO-1H-PYRROLO-[1,2-A]-IMIDAZOLE
6-ETHOXYCARBONYL-6-HYDROXY-7-(4-METHOXYBENZOYL)-5-OXO-2,3,5,6-TETRAHYDRO-1H-PYRROLO-[1,2-A]-IMIDAZOLE
6-ETHOXYCARBONYL-6-HYDROXY-7-(4-METHYLBENZOYL)-5-OXO-2,3,5,6-TETRAHYDRO-1H-PYRROLO-[1,2-A]-IMIDAZOLE
7-ETHOXYCARBONYL-7-HYDROXY-1-METHYL-8-(4-METHOXY-BENZOYL)-6-OXO-1,2,3,4,6,7-HEXAHYDROPYRROLO-[1,2-A]-PYRIMIDINE
(+/-)-STRYCHNOXANTHINE-CHLORIDE
20-EPISTRYCHNOXANTHINE-CHLORIDE
Title Journal or Book Year
The aza-ene reaction of heterocyclic ketene aminals with activated carbonyl compounds: a novel and efficient synthesis of γ-lactam-fused diazaheterocycles Journal of the Chemical Society, Perkin Transactions 1 1999
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