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【结 构 式】 
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【分子编号】39322 【品名】5,5-bis([[tert-butyl(diphenyl)silyl]oxy]methyl)-3-[(E)-3-isopropyl-4-methylpentylidene]dihydro-2(3H)-furanone 【CA登记号】 |
【 分 子 式 】C47H62O4Si2 【 分 子 量 】747.17788 【元素组成】C 75.55% H 8.36% O 8.57% Si 7.52% |
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：(IXa)Aldol condensation of silylated lactone (VII) with aldehyde (IV) gave hydroxy lactone (VIII). Subsequent hydroxyl group mesylation followed by elimination in the presence of DBU generated alkylidene lactone (IXa-b) as a mixture of geometric isomers, which were separated by chromatography. Desilylation of (IX) to afford diol (X) was achieved by means of HF/pyridine. Finally, monoacylation of (X) with acid chloride (VI) and pyridine furnished the target ester.
| 【1】 Marquez, V.E.; Bienfait, B.; Lewin, N.E.; Benzaria, S.; Bhattacharyya, D.K.; Lee, J.; Nacro, K.; Han, K.-C.; Kang, J.-H.; Blumberg, P.M.; Conformationally constrained analogues of diacylglycerol (DAG). 16. How much structural complexity is necessary for recognition and high binding affinity to protein kinase C?. J Med Chem 2000, 43, 5, 921. |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (IXa) | 39322 | 5,5-bis([[tert-butyl(diphenyl)silyl]oxy]methyl)-3-[(E)-3-isopropyl-4-methylpentylidene]dihydro-2(3H)-furanone | C47H62O4Si2 | 详情 | 详情 | |
| (IXb) | 39323 | 5,5-bis([[tert-butyl(diphenyl)silyl]oxy]methyl)-3-[(Z)-3-isopropyl-4-methylpentylidene]dihydro-2-furanone | C47H62O4Si2 | 详情 | 详情 | |
| (IV) | 39317 | 3-isopropyl-4-methylpentanal | C9H18O | 详情 | 详情 | |
| (VI) | 39319 | 3-isopropyl-4-methylpentanoyl chloride | C9H17ClO | 详情 | 详情 | |
| (VII) | 39320 | 5,5-bis([[tert-butyl(diphenyl)silyl]oxy]methyl)dihydro-2(3H)-furanone | C38H46O4Si2 | 详情 | 详情 | |
| (VIII) | 39321 | 5,5-bis([[tert-butyl(diphenyl)silyl]oxy]methyl)-3-(1-hydroxy-3-isopropyl-4-methylpentyl)dihydro-2(3H)-furanone | C47H64O5Si2 | 详情 | 详情 | |
| (X) | 39324 | 5,5-bis(hydroxymethyl)-3-[(Z)-3-isopropyl-4-methylpentylidene]dihydro-2-furanone | C15H26O4 | 详情 | 详情 |
Extended Information