【结 构 式】 |
【分子编号】39001 【品名】methyl 5-(bromomethyl)-2'-methyl[1,1'-biphenyl]-2-carboxylate 【CA登记号】 |
【 分 子 式 】C16H15BrO2 【 分 子 量 】319.1979 【元素组成】C 60.21% H 4.74% Br 25.03% O 10.02% |
合成路线1
该中间体在本合成路线中的序号:(VI)Palladium-catalyzed coupling of dimethyl iodoterephthalate (I) with 2-methylphenylboronic acid (II) afforded biphenyl (III). Hydrolysis of (III) with LiOH yielded mono acid (IV), which was reduced to alcohol (V) using borane in cold THF. Subsequent reaction of (V) with PBr3 furnished the intermediate bromide (VI).
【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 |
---|---|---|---|---|---|---|
(I) | 38996 | dimethyl 2-iodoterephthalate | C10H9IO4 | 详情 | 详情 | |
(II) | 38997 | 2-methylphenylboronic acid | 16419-60-6 | C7H9BO2 | 详情 | 详情 |
(III) | 38998 | dimethyl 2'-methyl[1,1'-biphenyl]-2,5-dicarboxylate | C17H16O4 | 详情 | 详情 | |
(IV) | 38999 | 6-(methoxycarbonyl)-2'-methyl[1,1'-biphenyl]-3-carboxylic acid | C16H14O4 | 详情 | 详情 | |
(V) | 39000 | methyl 5-(hydroxymethyl)-2'-methyl[1,1'-biphenyl]-2-carboxylate | C16H16O3 | 详情 | 详情 | |
(VI) | 39001 | methyl 5-(bromomethyl)-2'-methyl[1,1'-biphenyl]-2-carboxylate | C16H15BrO2 | 详情 | 详情 |
合成路线2
该中间体在本合成路线中的序号:(VI)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.
【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 |