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【结 构 式】

【分子编号】20195

【品名】1(S)-[5(R)-[5(R)-(1(R),2-Epoxyethyl)tetrahydrofuran-2(R)-yl]tetrahydrofuran-2(R)-yl]undecan-1-ol

【CA登记号】

【 分 子 式 】C21H38O4

【 分 子 量 】354.53032

【元素组成】C 71.15% H 10.8% O 18.05%

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:(XX)

2) The reduction of (XIV) with DIBAL followed by protection with methoxymethyl chloride (MOM-Cl) yields the methoxymethyl ether (XV), which by regioselective dihydroxylation with AD-mix-beta, followed by mesylation with mesyl chloride affords the dimesylate (XVI). A new regioselective dihydroxylation of (XVI) with AD-mix-beta gives the diol (XVII), which is cyclized by treatment first with p-toluenesulfonic acid and then by heating at 140 C in pyridine yielding the bis(tetrahydrofuran) derivative (XVIII). The deprotection of (XVIII) with boron trilfuoride.ethearate, followed by tosylation with tosyl chloride in pyridine affords the tosylate (XIX), which is cyclized to the epoxide (XX) by reaction with K2CO3 in methanol. The acetylation of the secondary alcohol of (XIX) with acetic anhydride in pyridine affords the acetate (XXI), which is condensed with trimethylsilylacetylene (XXII) by means of n-BuLi in THF giving the acetylenic alcohol (XXIII).

1 Yazbak, A.; et al.; Total synthesis of uvaricin. J Org Chem 1998, 63, 17, 5863.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XIV) 20188 ethyl (2E,6E)-9-[(4R,5S)-5-decyl-2,2-dimethyl-1,3-dioxolan-4-yl]-2,6-nonadienoate C26H46O4 详情 详情
(XV) 20190 (2E,6E)-9-[(4R,5S)-5-decyl-2,2-dimethyl-1,3-dioxolan-4-yl]-2,6-nonadienyl methoxymethyl ether; (4S,5R)-4-decyl-5-[(3E,7E)-9-(methoxymethoxy)-3,7-nonadienyl]-2,2-dimethyl-1,3-dioxolane C26H48O4 详情 详情
(XVI) 20191 (4S,5R)-4-decyl-5-((3S,4S,7E)-9-(methoxymethoxy)-3,4-bis[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-7-nonenyl)-2,2-dimethyl-1,3-dioxolane; (E,6S,7S)-9-[(4R,5S)-5-decyl-2,2-dimethyl-1,3-dioxolan-4-yl]-6,7-bis[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-2-nonenyl methoxymethyl ether C32H62O6S2 详情 详情
(XVII) 20192 (4S,5S,8R,9R)-4-[2-[(4R,5S)-5-decyl-2,2-dimethyl-1,3-dioxolan-4-yl]ethyl]-2-methyl-5-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-2-methylene-3,11,13-trioxa-2lambda(6)-thia-1-tetradecene-8,9-diol C32H64O8S2 详情 详情
(XVIII) 20193 1(S)-[5(R)-[5(R)-[1(R)-Hydroxy-2-(methoxymethoxy)ethyl]tetrahydrofuran-2(R)-yl]tetrahydrofuran-2(R)-yl]undecan-1-ol C23H44O6 详情 详情
(XIX) 20194 1(S)-[5(R)-[5(R)-[1(R)-Hydroxy-2-(p-toluenesulfonyloxy)ethyl]tetrahydrofuran-2(R)-yl]tetrahydrofuran-2(R)-yl]undecan-1-ol C28H46O7S 详情 详情
(XX) 20195 1(S)-[5(R)-[5(R)-(1(R),2-Epoxyethyl)tetrahydrofuran-2(R)-yl]tetrahydrofuran-2(R)-yl]undecan-1-ol C21H38O4 详情 详情
(XXI) 20196 Acetic acid 1(S)-[5(R)-[5(R)-(1(R),2-Epoxyethyl)tetrahydrofuran-2(R)-yl]tetrahydrofuran-2(R)-yl]undecyl ester C23H40O5 详情 详情
(XXII) 23897 ethynyl(trimethyl)silane;trimethylsilyl acetylene 1066-54-2 C5H10Si 详情 详情
(XXIII) 20198 Acetic acid 1(S)-[5(R)-[5(R)-(1(R)-hydoxy-3-butynyl)tetrahydrofuran-2(R)-yl]tetrahydrofuran-2(R)-yl]undecyl ester C25H42O5 详情 详情
(XXIV) 20205 (5S)-3-[(E)-9-iodo-8-nonenyl]-5-methyl-3-(phenylsulfanyl)dihydro-2(3H)-furanone C20H27IO2S 详情 详情
Extended Information