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【结 构 式】

【分子编号】54723

【品名】(1S,2S,4S)bicyclo[2.2.1]hept-5-ene-2-carbonyl chloride

【CA登记号】

【 分 子 式 】C8H9ClO

【 分 子 量 】156.61156

【元素组成】C 61.35% H 5.79% Cl 22.64% O 10.22%

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:(V)

The asymmetric Diels-Alder cycloaddition of cyclopentadiene (II) with the acrylic ester (I) of the chiral auxiliary D-pantolactone catalyzed by TiCl4 gives the chiral norbornene (III), which is treated with LiOH or NaOH to eliminate the auxiliary to yield the carboxylic acid (IV). The reaction of (IV) with oxalyl chloride affords the acyl chloride (V), which is condensed with 5,6-diamino-1,3-dipropyluracil (VI) by means of DMAP in pyridine to provide the amide (VII). The cyclization of (VII) by means of NaOH in dioxane gives the 1,3-dipropylxanthine derivative (VIII), which is finally epoxidated by means of magnesium monoperphthalate (MMPP) in aq. isopropanol to furnish the target xanthine derivative.

1 Pfister, J.R.; et al.; Synthesis and biological evaluation of the enantiomers of the potent and selective A1-adenosine antagonist 1, 3-dipropyl-8-[2-(5,6-epoxynorbonyl)]xanthine. J Med Chem 1997, 40, 12, 1773.
2 Belardinelli, L.; Olsson, R.; Baker, S.; Scammells, P.J.; Milner, P.G.; Pfister, J.R.; Schreiner, G.F. (University of Florida); Novel A1 adenosine receptor agonists and antagonists. EP 0725782; JP 1997507052; US 5446046; WO 9511904 .
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) 54720 (3R)-2,2-dimethyl-4-oxotetrahydro-3-furanyl acrylate C9H12O4 详情 详情
(II) 11183 1,3-Cyclopentadiene C5H6 详情 详情
(III) 54721 (3R)-2,2-dimethyl-4-oxotetrahydro-3-furanyl (1S,2S,4S)bicyclo[2.2.1]hept-5-ene-2-carboxylate C14H18O4 详情 详情
(IV) 54722 (1S,2S,4S)bicyclo[2.2.1]hept-5-ene-2-carboxylic acid C8H10O2 详情 详情
(V) 54723 (1S,2S,4S)bicyclo[2.2.1]hept-5-ene-2-carbonyl chloride C8H9ClO 详情 详情
(VI) 14628 5,6-diamino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedione C10H18N4O2 详情 详情
(VII) 54724 (1S,2S,4S)-N-(6-amino-2,4-dioxo-1,3-dipropyl-1,2,3,4-tetrahydro-5-pyrimidinyl)bicyclo[2.2.1]hept-5-ene-2-carboxamide C18H26N4O3 详情 详情
(VIII) 54725 8-[(1S,2S,4S)bicyclo[2.2.1]hept-5-en-2-yl]-1,3-dipropyl-3,9-dihydro-1H-purine-2,6-dione C18H24N4O2 详情 详情
Extended Information