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【结 构 式】 
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【分子编号】47128 【品名】2-chloro-2-methylpropane 【CA登记号】507-20-0 |
【 分 子 式 】C4H9Cl 【 分 子 量 】92.56816 【元素组成】C 51.9% H 9.8% Cl 38.3% |
合成路线1
该中间体在本合成路线中的序号：(II)2) By condensation of (E)-N-methyl-N-(1-naphthylmethyl)-N-(pent-2-en-4-ynyl)amine (I) with [14C]-tert-butyl-chloride (II) by means of butyllithium and diethylaluminum chloride in hexane-dichloromethane.
| 【1】 Andres, H.; Carbon-14 labelling of terbinafine, an antimycotic agent. J Label Compd Radiopharm 1989, 27, 11, 1307. |
合成路线2
该中间体在本合成路线中的序号：(III)Esterification of pyrrole-2-carboxylic acid (I) by treatment with TMSCl in MeOH yields methyl carboxylate (II), which is then condensed with tert-butyl chloride (III) by means of AlCl3 in 1,2-dichloroethane to provide methyl 5-tert-butyl pyrrole-2-carboxylate (IV). Nitration of pyrrolic derivative (IV) by reaction with HNO3/H2SO4 affords a mixture of compounds from which 3-nitropyrrole derivative (V) is cromatographically separated. Hydrogenation of (V) over Pd/C in MeOH allows conversion of the nitro group into an amino group to furnish methyl 3-amino-5-tert-butylpyrrole-2-carboxylate (VI), which is finally coupled to 2,3-dichlorophenyl isocyanate (VII) in dichloromethane to afford the desired compound.
| 【1】 Johnson, J.S.; Dally, R.; Redman, A.M.; et al.; p38 Kinase inhibitors for the treatment of arthritis and osteoporosis: Thienyl, furyl, and pyrrolyl ureas. Bioorg Med Chem Lett 2001, 11, 1, 9. |
| 【2】 Gunn, D.; Ranges, G.; Chen, J.; Bombara, M.; Scott, W.; Rauner, D.; Redman, A.; Paulsen, H.; Smith, R.; Renick, J. (Bayer Corp.); Inhibition of p38 kinase activity by aryl ureas. WO 9852558 . |
| 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) | 31796 | Pyrrole-2-carboxylic acid; 1H-pyrrole-2-carboxylic acid | 634-97-9 | C5H5NO2 | 详情 | 详情 |
| (II) | 45616 | methyl 1H-pyrrole-2-carboxylate | C6H7NO2 | 详情 | 详情 | |
| (III) | 47128 | 2-chloro-2-methylpropane | 507-20-0 | C4H9Cl | 详情 | 详情 |
| (IV) | 47129 | methyl 5-(tert-butyl)-1H-pyrrole-2-carboxylate | C10H15NO2 | 详情 | 详情 | |
| (V) | 47130 | methyl 5-(tert-butyl)-3-nitro-1H-pyrrole-2-carboxylate | C10H14N2O4 | 详情 | 详情 | |
| (VI) | 47131 | methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylate | C10H16N2O2 | 详情 | 详情 | |
| (VII) | 29667 | N-(2-chloroethyl)-N-[2-(3-methoxyphenyl)-1-methylethyl]-N-methylamine; N-(2-chloroethyl)-1-(3-methoxyphenyl)-N-methyl-2-propanamine | C13H20ClNO | 详情 | 详情 |