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【结 构 式】 
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【分子编号】25447 【品名】4-phenyl-4-piperidinecarboxylic acid 【CA登记号】3627-45-0 |
【 分 子 式 】C12H15NO2 【 分 子 量 】205.25664 【元素组成】C 70.22% H 7.37% N 6.82% O 15.59% |
合成路线1
该中间体在本合成路线中的序号：(I)This compound can be obtained by two related ways: 1.- The reduction of 4-phenylpiperidine-4-carboxylic acid (I) with LiAlH4 in THF gives the corresponding methanol derivative (II), which is treated with tert-butoxycarbonyl anhydride in THF to yield the N-protected piperidine (III). The acylation of (III) with 3,5-bis(trifluoromethyl)benzyl bromide (IV) by means of NaH in DMF affords the corresponding ether (V), which is deprotected with HCl in ethyl ether to afford the free piperidine (VI) (1,2). Finally, (VI) is reductocondensed with 2-methylthiazole-5-carbaldehyde (VII) by means of sodium cyanoborohydride in methanol/acetic acid. 2.- The piperidine derivative (VI) can also be condensed with 5-(bromomethyl)-2-methylthiazole (VIII) by means of K2CO3 in DMF.
| 【1】 Stevenson, G.I.; Huscroft, I.; Macleod, A.M.; Swain, C.J.; Cascieri, M.A.; Chicchi, G.G.; Graham, M.I.; Harrison, T.; Kelleher, F.J.; Kurtz, M.; Ladduwahetty, T.; Merchant, K.J.; Metzger, J.M.; MacIntyre, D.E.; Sadowski, S.; Sohal, B.; Owens, A.P.; 4,4-Disubstituted piperidine high-affinity NK1 antagonists: Structure-activity relationships and in vivo activity. J Med Chem 1998, 41, 23, 4623. |
| 【2】 Harrison, T.; Mcleod, A.M.; Stevenson, G.I.; Williams, B.J. (Merck Sharp & Dohme Ltd.); 4-Arylmethyloxymethyl piperidines as tachykinin antagonists. EP 0666856; JP 1996502510; US 5620989; WO 9410165 . |
| 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) | 25447 | 4-phenyl-4-piperidinecarboxylic acid | 3627-45-0 | C12H15NO2 | 详情 | 详情 |
| (II) | 27675 | (4-phenyl-4-piperidinyl)methanol | C12H17NO | 详情 | 详情 | |
| (III) | 27676 | tert-butyl 4-(hydroxymethyl)-4-phenyl-1-piperidinecarboxylate | C17H25NO3 | 详情 | 详情 | |
| (IV) | 27677 | 1-(bromomethyl)-3,5-bis(trifluoromethyl)benzene | 32247-96-4 | C9H5BrF6 | 详情 | 详情 |
| (V) | 27678 | tert-butyl 4-([[3,5-bis(trifluoromethyl)benzyl]oxy]methyl)-4-phenyl-1-piperidinecarboxylate | C26H29F6NO3 | 详情 | 详情 | |
| (VI) | 27679 | 3,5-bis(trifluoromethyl)benzyl (4-phenyl-4-piperidinyl)methyl ether | C21H21F6NO | 详情 | 详情 | |
| (VII) | 27680 | 2-methyl-1,3-thiazole-5-carbaldehyde | C5H5NOS | 详情 | 详情 | |
| (VIII) | 27681 | 5-(bromomethyl)-2-methyl-1,3-thiazole | C5H6BrNS | 详情 | 详情 |
合成路线2
该中间体在本合成路线中的序号：(VII)Condensation of 4-nitrobenzaldehyde (I) with N-methyl acetoacetamide (II) in the presence of piperidine acetate gave benzylideneacetoacetamide (III). This was further condensed with 2-cyanoethyl 3-amino-2-butenoate (IV) to provide dihydropyridine (V), which was resolved into the enantiomers using chiral HPLC. Then, basic hydrolysis of the cyanoethyl ester from the appropriate enantiomer of (V) yielded carboxylic acid (VI). The aminopropyl piperidine (X) was obtained by esterification of 4-phenyl-4-piperidinecarboxylic acid (VII) with MeOH and H2SO4, followed by alkylation of piperidine (VIII) with 3-bromopropylamine (IX). Finally, amine (X) was coupled to acid (VI) by means of EDC and DMAP to furnish the target compound.
| 【1】 Nagarathnam, D.; Wetzel, J.M.; Miao, S.W.; Marzabadi, M.R.; Chiu, G.; Wong, W.C.; Hong, X.; Fang, J.; Forray, C.; Branchek, T.A.; Heydorn, W.E.; Chang, R.S.; Broten, T.; Schorn, T.W.; Gluchowski, C.; Design and synthesis of novel alpha1a adrenoceptor-selective dihydropyridine antagonists for the treatment of benign prostatic hyperplasia. J Med Chem 1998, 41, 26, 5320. |
| 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) | 18184 | 4-Nitrobenzaldehyde | 555-16-8 | C7H5NO3 | 详情 | 详情 |
| (II) | 25443 | N-methyl-3-oxobutanamide | 20306-75-6 | C5H9NO2 | 详情 | 详情 |
| (III) | 25444 | (Z)-2-acetyl-N-methyl-3-(4-nitrophenyl)-2-propenamide | C12H12N2O4 | 详情 | 详情 | |
| (IV) | 13987 | 2-cyanoethyl (E)-3-amino-2-butenoate | C7H10N2O2 | 详情 | 详情 | |
| (V) | 25445 | 2-cyanoethyl 2,6-dimethyl-5-[(methylamino)carbonyl]-4-(4-nitrophenyl)-1,4-dihydro-3-pyridinecarboxylate | C19H20N4O5 | 详情 | 详情 | |
| (VI) | 25446 | 2,6-dimethyl-5-[(methylamino)carbonyl]-4-(4-nitrophenyl)-1,4-dihydro-3-pyridinecarboxylic acid | C16H17N3O5 | 详情 | 详情 | |
| (VII) | 25447 | 4-phenyl-4-piperidinecarboxylic acid | 3627-45-0 | C12H15NO2 | 详情 | 详情 |
| (VIII) | 25448 | methyl 4-phenyl-4-piperidinecarboxylate | C13H17NO2 | 详情 | 详情 | |
| (IX) | 25449 | 3-bromo-1-propanamine; 3-bromopropylamine | 18370-81-5 | C3H8BrN | 详情 | 详情 |
| (X) | 25450 | methyl 1-(3-aminopropyl)-4-phenyl-4-piperidinecarboxylate | C16H24N2O2 | 详情 | 详情 |