N-(2-cyclohexylethyl)-1-butanamine; N-butyl-N-(2-cyclohexylethyl)amine -Drug Synthesis Database

【结构式】

【分子编号】39004

【品名】N-(2-cyclohexylethyl)-1-butanamine; N-butyl-N-(2-cyclohexylethyl)amine

【CA登记号】

【分子式】C₁₂H₂₅N

【分子量】183.33724

【元素组成】C 78.62% H 13.74% N 7.64%

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：(IX)

Cyclohexylacetic acid (VII) was converted to acid chloride and then condensed with n-butyl amine to give amide (VIII). Reduction of (VIII) with LiAlH4 afforded secondary amine (IX), which was alkylated with bromide (VI) yielding amino ester (X). After basic hydrolysis of the ester group of (X), the resultant carboxylic acid (XI) was coupled with L-methionine methyl ester (XII) to produce amide (XIII). The methyl ester group of (XIII) was finally hydrolyzed by treatment with LiOH.

参考文献中间体

合成目标

【1】 Donner, B.G.; Janowick, D.A.; Larsen, J.J.; Rosenberg, S.H.; Hamilton, A.D.; Barr, K.J.; Sorensen, B.K.; Augeri, D.J.; Kalvin, D.M.; O'Connor, S.J.; Fakhoury, S.A.; Swenson, R.E.; Liu, G.; Sebti, S.M.; Shen, W. (University of Pittsburgh); Inhibitors of protein isoprenyl transferases. EP 0986384; WO 9850029; WO 9850030; WO 9850031 .

中间体序号	中间体编号	品名	CAS号	分子式	供应商	用于合成
(VI)	39001	methyl 5-(bromomethyl)-2'-methyl[1,1'-biphenyl]-2-carboxylate		C₁₆H₁₅BrO₂	详情	详情
(VII)	39002	2-cyclohexylacetic acid	5292-21-7	C₈H₁₄O₂	详情	详情
(VIII)	39003	N-butyl-2-cyclohexylacetamide		C₁₂H₂₃NO	详情	详情
(IX)	39004	N-(2-cyclohexylethyl)-1-butanamine; N-butyl-N-(2-cyclohexylethyl)amine		C₁₂H₂₅N	详情	详情
(X)	39005	methyl 5-[[butyl(2-cyclohexylethyl)amino]methyl]-2'-methyl[1,1'-biphenyl]-2-carboxylate		C₂₈H₃₉NO₂	详情	详情
(XI)	39006	5-[[butyl(2-cyclohexylethyl)amino]methyl]-2'-methyl[1,1'-biphenyl]-2-carboxylic acid		C₂₇H₃₇NO₂	详情	详情
(XII)	17950	D-Methionine methyl ester; methyl (2S)-2-amino-4-(methylsulfanyl)butanoate hydrochloride	21691-49-6	C₆H₁₃NO₂S	详情	详情
(XIII)	39007	methyl (2S)-2-[[(5-[[butyl(2-cyclohexylethyl)amino]methyl]-2'-methyl[1,1'-biphenyl]-2-yl)carbonyl]amino]-4-(methylsulfanyl)butanoate		C₃₃H₄₈N₂O₃S	详情	详情

Extended Information