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【结 构 式】

【分子编号】58262

【品名】ethyl 3-piperidinecarboxylate

【CA登记号】

【 分 子 式 】C8H15NO2

【 分 子 量 】157.21264

【元素组成】C 61.12% H 9.62% N 8.91% O 20.35%

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:(II)

The condensation of dibenzocycloheptylidene derivative (I) with radiolabelled piperidine-3-carboxylic acid ethyl ester (II) by means of K2CO3 in ethyl acetate gives the adduct (III), which is hydrolyzed with aqueous HCl to yield the carboxylic acid (IV). Finally, this compound is submitted to optical resolution by means of chiral chromatography to provide the chiral radiolabelled compound.

1 Valsborg, J.S.; Foged, C.; Radiolabelling of NNC 05-1869, a compound for treatment of diabetic neuropathy. J Label Compd Radiopharm 2002, 45, 4, 351.
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) 52139 5-(3-bromopropylidene)-10,11-dihydro-5H-dibenzo[a,d]cycloheptene C18H17Br 详情 详情
(II) 25693 ethyl 3-piperidinecarboxylate 5006-62-2 C8H15NO2 详情 详情
(II) 58262 ethyl 3-piperidinecarboxylate C8H15NO2 详情 详情
(III) 58263 ethyl 1-[3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)propyl]-3-piperidinecarboxylate C26H31NO2 详情 详情
(III) 58266 ethyl 1-[3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)propyl]-3-piperidinecarboxylate C26H31NO2 详情 详情
(IV) 58264 1-[3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)propyl]-3-piperidinecarboxylic acid C24H27NO2 详情 详情
(IV) 58265 1-[3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)propyl]-3-piperidinecarboxylic acid C24H27NO2 详情 详情
Extended Information