220844-96-2Relevant academic research and scientific papers
Consecutive reactions between methyl 3-dehydroshikimiate, amines and 1,2-dichloroalkanes under microwave conditions: A practical, one-pot construction of N-substituted dihydrobenzoxazines
Zhang, Ensheng,Xu, Tianlong,Wang, Dejian,Huang, Tongkun,Yuan, Mu,Li, Jun,Zou, Yong
, p. 10022 - 10027 (2014/03/21)
A biomass-involved, one-pot, two-step protocol for the synthesis of N-substituted 3,4-dihydro-2H-1,4-benzoxazines has been developed. A wide range of new compounds have been efficiently synthesized in moderate to excellent yields via the three-component consecutive reactions between methyl 3-dehydroshikimiate (3-MDHS), amines and 1,2-dichloroalkanes in short reaction times under microwave conditions.
An acid-catalyzed O,N-acyl migration and application to the synthesis of N-(4-isopropyl-2,2-dimethyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6- carbonyl) guanidine methanesulfonate (KB-R9032), a novel Na/H exchange inhibitor
Yamamoto, Takeshi,Hori, Manabu,Watanabe, Ikuo,Tsutsui, Hisayoshi,Ikeda, Shoji,Ohtaka, Hiroshi
, p. 22 - 27 (2007/10/03)
In the search for a practical synthesis of N-(4-isopropyl-2,2-dimethyl- 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6-carbonyl)guanidine methanesulfonate (KB-R9032), a potent Na/H exchange inhibitor, the acylation of methyl 4- hydroxy-3-isopropylaminobenzoate 6a with 2-bromoisobutyryl bromide was carried out in order to prepare an N-acyl derivative, 8a. However, an O-acyl derivative 7a was obtained selectively. Acylations of derivatives of 6a were examined. The results revealed that the O-acylation occurred because of the steric repulsion between the N-isopropyl moiety and the bulky acyl bromide. Then, we investigated the O,N-acyl migration of 7a. We found that the migration was catalyzed by carboxylic acid and that 8a was precipitated from a diisopropyl ether solution in good yield. Treatment of 8a with potassium carbonate and subsequent guanidine gave the synthetic intermediate for KB- R9032 in high yield.
