
Synthetic Communications p. 559 - 566 (1997)
Update date:2022-08-03
Topics:
Morie, Toshiya
Harada, Hiroshi
Kato, Shiro
The convenient large-scale synthesis of the title compound, which is the intermediate of potent 5-HT3 receptor antagonist, N-(1-benzyl)-4-methylhexahydro-1H-1,4-diazepin-6-yl)-1H-indazole-3 carboxamide (1), is described.
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(1997)Doi:10.1039/CC9960001623
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(1997)Doi:10.1021/jo102480s
(2011)Doi:10.1080/00397919708005035
(1997)Doi:10.1016/S0022-328X(00)86813-8
(1982)