【药物名称】AWD-12-343
化学结构式(Chemical Structure):
参考文献No.583863
标题:AWD 12-343, a new orally active PDE 4 inhibitor - Synthesis and comparison with SB 207499, rolipram and AWD 12-281
作者:H鰂gen, N.; et al.
来源:27th Natl Med Chem Symp (June 13 2000, Kansas City) 2000,Abst B-19
合成路线图解说明:

Alkylation of 5-fluoroindole (I) with 4-fluorobenzyl chloride (II) provided the N-benzyl indole (III). Subsequent reaction of (III) with oxalyl chloride furnished the indolylglyoxylic acid chloride (IV). This was finally coupled with 4-amino-3,5-dichloropyridine (V) to afford the corresponding amide.

参考文献No.593852
标题:AWD 12-343, a new orally active PDE 4 inhibitor - Synthesis and comparison with SB 207499, rolipram and AWD 12-281
作者:Egerland, U.; Kronbach, T.; H鰂gen, N.; Poppe, H.; K黶ters, S.; szelenyi, S.
来源:16th Int Symp Med Chem (Sept 18 2000, Bologna) 2000,Abst PA-79
合成路线图解说明:

Alkylation of 5-fluoroindole (I) with 4-fluorobenzyl chloride (II) provided the N-benzyl indole (III). Subsequent reaction of (III) with oxalyl chloride furnished the indolylglyoxylic acid chloride (IV). This was finally coupled with 4-amino-3,5-dichloropyridine (V) to afford the corresponding amide.

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