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【结 构 式】 
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【分子编号】27760 【品名】tert-butyl 4-[([4-[4-(3-cyclopentylpropyl)-5-oxo-4,5-dihydro-1H-1,2,3,4-tetraazol-1-yl]phenyl]sulfonyl)amino]phenethyl[(2R)-2-hydroxy-2-(3-pyridinyl)ethyl]carbamate 【CA登记号】 |
【 分 子 式 】C35H45N7O6S 【 分 子 量 】691.85188 【元素组成】C 60.76% H 6.56% N 14.17% O 13.88% S 4.63% |
合成路线1
该中间体在本合成路线中的序号：(XXIV)Cyclopentylpropanol (XV) was converted to mesylate (XVI) and subsequently treated with NaI to give iodide (XVII). Then, alkylation of phenyltetrazolone (XIX), (obtained from phenyl isocyanate (XVIII) and aluminum azide), with iodide (XVII) afforded the substituted tetrazolone (XX). Nitration of the phenyl ring of (XX) employing nitronium tetrafluoborate produced the 4-nitro derivative (XXI) along with minor amounts of the 2-nitro isomer, which was separated by flash chromatography. After catalytic hydrogenation of the nitro group of (XXI) to aniline (XXII), diazotization, followed by treatment with an AcOH solution of SO2 in the presence of CuCl furnished sulfonyl chloride (XXIII). Coupling of this sulfonyl chloride with the intermediate amine (VII) in the presence of pyridine gave sulfonamide (XXIV). Finally, the Boc protecting group of (XXIV) was removed by acidic treatment to provide the title compound.
| 【1】 Shih, T.L.; Candelore, M.R.; Cascieri, M.A.; L-770,644: A potent and selective human beta3 adrenergic receptor agonist with improved oral bioavailability. Bioorg Med Chem Lett 1999, 9, 9, 1251. |
| 【2】 Fisher, M.H.; Naylor, E.M.; Ok, D.; Weber, A.E.; Shih, T.; Ok, H. (Merck & Co., Inc.); Substd. sulfonamides as selective beta3 agonists for the treatment of diabetes and obesity. EP 0757674; JP 1997512275; US 5541197; US 5561142; WO 9529159 . |
| 【3】 Smith, R.G. (Merck & Co., Inc.); Combination therapy for the treatment of diabetes and obesity. JP 1999515027; WO 9716189 . |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (VII) | 26553 | tert-butyl 4-aminophenethyl[(2R)-2-hydroxy-2-(3-pyridinyl)ethyl]carbamate | C20H27N3O3 | 详情 | 详情 | |
| (XV) | 27752 | 3-cyclopentyl-1-propanol | 767-05-5 | C8H16O | 详情 | 详情 |
| (XVI) | 27753 | 3-cyclopentylpropyl methanesulfonate | C9H18O3S | 详情 | 详情 | |
| (XVII) | 27754 | 1-(3-iodopropyl)cyclopentane | C8H15I | 详情 | 详情 | |
| (XVIII) | 11289 | 1-Isocyanatobenzene; phenyl isocyanate; Phenylisocyanate | 103-71-9 | C7H5NO | 详情 | 详情 |
| (XIX) | 27755 | 1-phenyl-1,4-dihydro-5H-1,2,3,4-tetraazol-5-one | C7H6N4O | 详情 | 详情 | |
| (XX) | 27756 | 1-(3-cyclopentylpropyl)-4-phenyl-1,4-dihydro-5H-1,2,3,4-tetraazol-5-one | C15H20N4O | 详情 | 详情 | |
| (XXI) | 27757 | 1-(3-cyclopentylpropyl)-4-(4-nitrophenyl)-1,4-dihydro-5H-1,2,3,4-tetraazol-5-one | C15H19N5O3 | 详情 | 详情 | |
| (XXII) | 27758 | 1-(4-aminophenyl)-4-(3-cyclopentylpropyl)-1,4-dihydro-5H-1,2,3,4-tetraazol-5-one | C15H21N5O | 详情 | 详情 | |
| (XXIII) | 27759 | 4-[4-(3-cyclopentylpropyl)-5-oxo-4,5-dihydro-1H-1,2,3,4-tetraazol-1-yl]benzenesulfonyl chloride | C15H19ClN4O3S | 详情 | 详情 | |
| (XXIV) | 27760 | tert-butyl 4-[([4-[4-(3-cyclopentylpropyl)-5-oxo-4,5-dihydro-1H-1,2,3,4-tetraazol-1-yl]phenyl]sulfonyl)amino]phenethyl[(2R)-2-hydroxy-2-(3-pyridinyl)ethyl]carbamate | C35H45N7O6S | 详情 | 详情 |