【药物名称】Motrazepam, Ro-06-9098/000
化学结构式(Chemical Structure):
参考文献No.900419
标题:
作者:Hellerbach, J.; Walser, A.
来源:AU 325050; CA 971960; CA 978548; CA 980344; CH 562220; CH 573926; FR 2034550; GB 1306451; GB 1306452; GB 1306453; GB 1306454; US 7886214; ZA 7000709
合成路线图解说明:

By reacting 1,3-dihydro-7-nitro-5-phenyl-2H-1,4-benzodiazepin-2-one (I) with sodium methoxide (A) and chloromethylmethylether in dimethylformamide (1); by treating the 4,5-dihydro-4-p-tolylsulfonyl derivative (II) with sodium methoxide in dimethyl formamide (2) or by heating the 4-hydroxy derivative (III) in toluene containing dicyclohexylcarbodiimide (3).

参考文献No.900420
标题:
作者:Hellerbach, J.; Walser, A.
来源:CH 574442
合成路线图解说明:

By reacting 1,3-dihydro-7-nitro-5-phenyl-2H-1,4-benzodiazepin-2-one (I) with sodium methoxide (A) and chloromethylmethylether in dimethylformamide (1); by treating the 4,5-dihydro-4-p-tolylsulfonyl derivative (II) with sodium methoxide in dimethyl formamide (2) or by heating the 4-hydroxy derivative (III) in toluene containing dicyclohexylcarbodiimide (3).

参考文献No.900421
标题:
作者:Hellerbach, J.; Walser, A.
来源:CH 574420
合成路线图解说明:

By reacting 1,3-dihydro-7-nitro-5-phenyl-2H-1,4-benzodiazepin-2-one (I) with sodium methoxide (A) and chloromethylmethylether in dimethylformamide (1); by treating the 4,5-dihydro-4-p-tolylsulfonyl derivative (II) with sodium methoxide in dimethyl formamide (2) or by heating the 4-hydroxy derivative (III) in toluene containing dicyclohexylcarbodiimide (3).

参考文献No.950177
标题:Motrazepam
作者:Unterhalt, B.
来源:Drugs Fut 1978,3(10),758
合成路线图解说明:

By reacting 1,3-dihydro-7-nitro-5-phenyl-2H-1,4-benzodiazepin-2-one (I) with sodium methoxide (A) and chloromethylmethylether in dimethylformamide (1); by treating the 4,5-dihydro-4-p-tolylsulfonyl derivative (II) with sodium methoxide in dimethyl formamide (2) or by heating the 4-hydroxy derivative (III) in toluene containing dicyclohexylcarbodiimide (3).

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