Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles

Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2012, Volume: 22, Number: 2, Pages: 85-86 Pages count : 2 DOI: 10.1016/j.mencom.2012.03.011

Authors

Kislyi Victor P. ¹ , Danilova Evgenia B. ¹ , Semenov Victor V. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Treatment of 5-benzoyl-4-(iodoacetylamino)isoxazoles with alcoholic ammonia leads to isoxazolo[4,5-e][1,4]diazepin-5-ones, whereas the analogous chloroacetylamino derivatives are converted into a mixture of the deacylated 4-aminoisoxazoles and isoxazolo- [4,5-d]pyrimidines.

Kislyi V.P. , Danilova E.B. , Semenov V.V.
Synthesis of isoxazolo[4,5-e][1,4]diazepin-5-ones from 5-acyl-4-(haloacetylamino)isoxazoles
Mendeleev Communications. 2012. V.22. N2. P.85-86. DOI: 10.1016/j.mencom.2012.03.011 WOS Scopus OpenAlex

Web of science:	WOS:000303692100011
Scopus:	2-s2.0-84859571539
OpenAlex:	W2025344412

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