NEW FACILE ALKOXYCARBONYLATING AGENT, ALKYL PYRAZOLE-1-CARBOXYLATES -THE PREPARATION AND THE UTILITIES

Citation
C. Kashima et al., NEW FACILE ALKOXYCARBONYLATING AGENT, ALKYL PYRAZOLE-1-CARBOXYLATES -THE PREPARATION AND THE UTILITIES, Tetrahedron, 54(49), 1998, pp. 14679-14688
Citations number
26
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404020
Volume
54
Issue
49
Year of publication
1998
Pages
14679 - 14688
Database
ISI
SICI code
0040-4020(1998)54:49<14679:NFAAAP>2.0.ZU;2-G
Abstract
Alkyl pyrazole-1-carboxylates (2), which were readily prepared from al kyl chloroformate or carbazate in good yields, were provided as the ne w facile alkoxycarbonylating agents toward the Grignard reagents for t he synthesis of one carbon higher carboxylic esters. Also amines were alkoxycarbonylated by 2 to produce the corresponding urethanes even in an aqueous medium. Benzyl 3,5-dimethylpyrazole-1-carboxylate (2d) cou ld be utilized for the Cbz-protection of amino acids and esters in goo d yield without any racemization. (C) 1998 Elsevier Science Ltd. All r ights reserved.