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【结 构 式】

【分子编号】20551

【品名】1-(2-oxopropyl)-3-propyl-8-tricyclo[3.3.1.0(3,7)]non-3-yl-3,7-dihydro-1H-purine-2,6-dione

【CA登记号】

【 分 子 式 】C20H26N4O3

【 分 子 量 】370.4516

【元素组成】C 64.85% H 7.07% N 15.12% O 12.96%

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:(XI)

The selective biological hydroxylation of compounds (XI) by means of Absidia ramosa FERM BP-4605 in corn steep liquor, glucose, Brig 35 at 28 C, 5-7 days gives metabolites M3.

1 Shimada, J.; Eguchi, T.; Yasuzawa, T.; Nakamura, A.; Horiguchi, A.; Mochida, K.; Suzuki, F.; Synthesis of rat metabolites of a adenosine A1 antagonist, KW-3902. Symp Med Chem 1996, Abst 1-P-24.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
M3 63838 8-(9-hydroxytricyclo[3.3.1.0~3,7~]non-3-yl)-1-(2-oxopropyl)-3-propyl-3,7-dihydro-1H-purine-2,6-dione C20H26N4O4 详情 详情
(XI) 20551 1-(2-oxopropyl)-3-propyl-8-tricyclo[3.3.1.0(3,7)]non-3-yl-3,7-dihydro-1H-purine-2,6-dione C20H26N4O3 详情 详情
Extended Information