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【结 构 式】

【分子编号】39021

【品名】(3aR,4S,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carbonyl chloride

【CA登记号】

【 分 子 式 】C13H14ClN5O4

【 分 子 量 】339.73816

【元素组成】C 45.96% H 4.15% Cl 10.44% N 20.61% O 18.84%

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 oxidation of 2',3'-isopropylideneadenosine (I) with potassium permanganate gives 2',3'-isopropylideneadenosine-5'-carboxylic acid (II) which with SOCl2 affords 2',3'-isopropylideneadenosine-5'-carbonyl chloride (III), which is treated first with dry liquid ethylamine and then hydrolyzed with aqueous hydrochloric acid.

1 Stein, H.H.; Prasad, R.N.; US 4029884 .
2 Stein, H.H.; Prasad, R.N.; US 3830796 .
3 Stein, H.H.; Prasad, R.N.; US 3914414 .
4 Stein, H.H.; Prasad, R.N.; US 3914415 .
5 Stein, H.H.; Prasad, R.N; US 3931401 .
6 Serradell, M.N.; Blancafort, P.; Castaner, J.; Hopkins, S.J.; NECA. Drugs Fut 1981, 6, 10, 627.
7 Stein, H.H.; Prasad, R.N.; US 3966917 .
8 Tietje, K.; Prasad, R.N.; N1,N6-Etheno-adenosine 5'-(N-ethylcarboxamide). Nucleic Acid Chemistry 1978, 2, 701-707.
9 Harman, R.E.; et al.; Permanganate oxidation of purine nucleosides. Chem Ind 1969, 1141.
10 Savic, M.; Brondyk, H.; Egan, R.S.; Bariana, D.S.; Fung, A.; Tietje, K.; Prasad, R.N.; Stein, H.H.; Modifications of the 5' position of purine nucleosides. 2. Synthesis and some cardiovascular properties of adenosine-5'-(N-substituted)carboxamides. J Med Chem 1980, 23, 3, 313-319.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(A) 10928 Ethanamine 75-04-7 C2H7N 详情 详情
(I) 17560 [(3aR,4R,6R,6aS)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]methanol 362-75-4 C13H17N5O4 详情 详情
(II) 39020 (3aR,4S,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carboxylic acid C13H15N5O5 详情 详情
(III) 39021 (3aR,4S,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole-4-carbonyl chloride C13H14ClN5O4 详情 详情
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