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【结 构 式】

【分子编号】34337

【品名】ethyl (3aR,7aS)-2-(5-methoxy-5-oxopentanoyl)-2,3,3a,4,7,7a-hexahydro-1H-indene-2-carboxylate

【CA登记号】

【 分 子 式 】C18H26O5

【 分 子 量 】322.40144

【元素组成】C 67.06% H 8.13% O 24.81%

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:(III)

The condensation of ethyl bicyclo[4.3.0]nona-3-ene-8-carboxylate (I) with methyl 4-chloroformylbutanoate (II) by means of lithium diisopropylamide in THF yields the ketodiester (III), which is reduced with NaBH4 in methanol to the hydroxydiester (IV). Acetylation of (IV) in the usual way affords the acetate (V), which is submitted to ozonolysis with O3 to give the dialdehyde (VI). The intramolecular aldol condensation of (VI) by means of Zn++ yields the desired hydroxyaldehyde (VII), which is submitted to a Horner-Wittig condensation with 2-oxoheptylidenetributylphosphorane (VIII) affording the enone (IX). The protection of the enone (X) with dihydropyran as usual yields the tetrahydropyranylether (X), which is reduced with NaSH4 in methanol to the unsaturated alcohol (Xl).

1 Sakai, K.; Amemiya, S.; Kojima, K.; A novel synthesis (±)-carbacyclin. Chem Pharm Bull 1984, 32, 4, 1349-54.
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) 34336 ethyl (3aR,7aS)-2,3,3a,4,7,7a-hexahydro-1H-indene-2-carboxylate C12H18O2 详情 详情
(II) 20650 methyl 5-chloro-5-oxopentanoate; methyl-4-chloroformylbutyrate 1501-26-4 C6H9ClO3 详情 详情
(III) 34337 ethyl (3aR,7aS)-2-(5-methoxy-5-oxopentanoyl)-2,3,3a,4,7,7a-hexahydro-1H-indene-2-carboxylate C18H26O5 详情 详情
(IV) 34338 ethyl (3aR,7aS)-2-(1-hydroxy-5-methoxy-5-oxopentyl)-2,3,3a,4,7,7a-hexahydro-1H-indene-2-carboxylate C18H28O5 详情 详情
(V) 34339 ethyl (3aR,7aS)-2-[1-(acetoxy)-5-methoxy-5-oxopentyl]-2,3,3a,4,7,7a-hexahydro-1H-indene-2-carboxylate C20H30O6 详情 详情
(VI) 34340 ethyl (3R,4S)-1-[1-(acetoxy)-5-methoxy-5-oxopentyl]-3,4-bis(2-oxoethyl)cyclopentanecarboxylate C20H30O8 详情 详情
(VII) 34341 ethyl (3aS,4R,5R,6aS)-2-[1-(acetoxy)-5-methoxy-5-oxopentyl]-4-formyl-5-hydroxyoctahydro-2-pentalenecarboxylate C20H30O8 详情 详情
(VIII) 34342 1-(tributylphosphoranylidene)-2-heptanone C19H39OP 详情 详情
(IX) 34343 ethyl (3aS,4S,5R,6aS)-2-[1-(acetoxy)-5-methoxy-5-oxopentyl]-5-hydroxy-4-[(E)-3-oxo-1-octenyl]octahydro-2-pentalenecarboxylate C27H42O8 详情 详情
(X) 34344 ethyl (3aS,4S,5R,6aR)-2-[1-(acetoxy)-5-methoxy-5-oxopentyl]-4-[(E)-3-oxo-1-octenyl]-5-[(tetrahydro-2H-pyran-2-yloxy)methyl]octahydro-2-pentalenecarboxylate C33H52O9 详情 详情
Extended Information