Ethyl bromoacetate → HCID 19738222, compound
Reaction equation
C(O)(=O)C.[OH:5][C:6]1[N:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[N:9]=[C:8]([CH3:17])[C:7]=1[CH:18]=O.[CH2:20]([O:22][C:23](=[O:26])[CH2:24]Br)[CH3:21]>>[CH3:17][C:8]1[C:7]2[CH:18]=[C:24]([C:23]([O:22][CH2:20][CH3:21])=[O:26])[O:5][C:6]=2[N:10]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:9]=1Participants
Procedure
Furo[2,3-c]pyrazole compounds were first synthesized by two of the present inventors, L. J. Haung and S. C. Kuo, and H. T. Li in an article published in J. Taiwan Pharm. Assoc. 31 (1), 47-55 (1979). Ethyl 3-methyl-1-phenylfuro[2,3-c]pyrazole-5-carboxylate (3) was synthesized in this article. As shown in the following Scheme 1, chloro-3-methyl-1-phenylpyrazole-4-carboxaldehyde (1) and ethylglycolate (2) were condensed to form ethyl 3-methyl-1-phenylfuro[2,3-c]pyrazole-5-carboxylate (3); or 5-hydroxy-3-methyl-1-phenylpyrazole-4-carboxal-dehyde acetate (4) was reacted with ethylbromoacetate (5) to obtain the ethyl 3-methyl-1-phenylfuro[2,3-c]pyrazole-5-carboxylate (3). The product produced by these two methods are very low in yield and stability. Therefore, only one furo[2,3-c]pyrazole compound (3) was synthesized and no further investigation was conducted in the above-mentioned article. ##STR1##
Sources & evidence
- ORD record
- ord-5a83e11559364c8c9a53783bebb1431e
- Source dataset
- uspto-grants-1993_08
- Patent number
- US05240947
Reaction notes
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