Ring transformation of 5-amino (or acylamino)-6-hydroxy (or benzoyloxy)methylpyrimidin-4(3H)-ones into 1H-imidazoles

DOI: 10.1002/jhet.5570340310

Source and publish data:

Journal of Heterocyclic Chemistry p. 761 - 764 (1997)

Update date:2022-08-04

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Authors:

Ueda, Taisei

Asai, Satoko

Oiji, Khoji

Nagai, Shin-Ichi

Nagatsu, Akito

Sakakibara, Jinsaku

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Article abstract of DOI:10.1002/jhet.5570340310

Treatment of 5-acylamino-6-hydroxy (or benzoyloxy)methyl-3- phenylpyrimidin-4(3H)-one 5,10 with 5% aqueous sodium hydroxide in ethanol gave 2-alkyl-5-hydroxymethyl-4-phenylcarbamoyl-1H-imidazoles 7,11. Oxidation of 5-amino-6-henzoyloxymethyl-3-phenylpyrim

Full text of DOI:10.1002/jhet.5570340310

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