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【结 构 式】

【分子编号】34450

【品名】(2S)-2-(tritylamino)-3-(1-trityl-1H-imidazol-4-yl)-1-propanol

【CA登记号】

【 分 子 式 】C44H39N3O

【 分 子 量 】625.81328

【元素组成】C 84.45% H 6.28% N 6.71% O 2.56%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(III)

L-Histidine methyl ester (I) was protected as the bis(tritylated) derivative (II) upon treatment with triphenylmethyl chloride and Et3N. Reduction of the ester function of (III) with LiAlH4 afforded alcohol (III), which was coupled with cyclohexylmethyl bromide (IV) in the presence of NaH in DMF, yielding the cyclohexylmethyl ether (V). Finally, cleavage of the trityl protecting groups of (V) with HCl in THF provided the title compound as the dihydrochloride salt.

1 Gynther, J.; Laitinen, J.T.; Kotisaari, S.; Tuomisto, L.; Mannistö, P.T.; Kovalainen, J.T.; Christiaans, A.M.; Synthesis and in vitro pharmacology of a series of new chiral histamine H3-receptor ligands: 2-(R and S)-amino-3-(1H-imidazol-4(5)-yl)propyl ether derivatives. J Med Chem 1999, 42, 7, 1193.
2 Kovalainen, J.T.; et al.; Investigation of the stereospecificity of the histamine H3-receptor with a series of new enantiomeric ligands. 15th European Federation for Medicinal Chemistry International Symposium on Medicinal Chemistry (Sept 6 1998, Edinburgh) 1998, Abst P.34.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
28630 Triphenylchloromethane; 1-[Chloro(diphenyl)methyl]benzene; Trityl chloride 76-83-5 C19H15Cl 详情 详情
(I) 23048 methyl (2S)-2-amino-3-(1H-imidazol-4-yl)propanoate C7H11N3O2 详情 详情
(II) 34449 methyl (2S)-2-(tritylamino)-3-(1-trityl-1H-imidazol-4-yl)propanoate C45H39N3O2 详情 详情
(III) 34450 (2S)-2-(tritylamino)-3-(1-trityl-1H-imidazol-4-yl)-1-propanol C44H39N3O 详情 详情
(IV) 31767 1-(bromomethyl)cyclohexane 2550-36-9 C7H13Br 详情 详情
(V) 34451 N-[(1S)-2-(cyclohexylmethoxy)-1-[(1-trityl-1H-imidazol-4-yl)methyl]ethyl]-N-tritylamine; (2S)-1-(cyclohexylmethoxy)-N-trityl-3-(1-trityl-1H-imidazol-4-yl)-2-propanamine C51H51N3O 详情 详情
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