methyl 1-(3,3-dimethyl-2-oxopentanoyl)-2-piperidinecarboxylate -Drug Synthesis Database

【结构式】

【分子编号】60289

【品名】methyl 1-(3,3-dimethyl-2-oxopentanoyl)-2-piperidinecarboxylate

【CA登记号】

【分子式】C₁₄H₂₃NO₄

【分子量】269.34096

【元素组成】C 62.43% H 8.61% N 5.2% O 23.76%

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)

Acylation of methyl pipecolinate (I) with methyl oxalyl chloride (II) provides oxamate (III). Subsequent addition of 1,1-dimethylpropylmagnesium chloride (IV) to oxamate (III) gives rise to keto amide (V). The methyl ester group of (V) is then hydrolyzed by means of LiOH, yielding the intermediate carboxylic acid (VI)

参考文献中间体

合成目标

【1】 Hamilton, G.S.; Wu, Y.-Q.; Limburg, D.C.; Wilkinson, D.E.; Vaal ,M.J.; Li, J.-H.; Thomas, C.; Huang, W.; Sauer, H.; Ross, D.T.; Soni, R.; Chen, Y.; Guo, H.; Howorth, P.; Valentine, H.; Liang, S.; Spicer, D.; Fuller, M.; Steiner, J.P; Synthesis of N-glyoxyl prolyl and pipecolyl amides and thioesters and evaluation of their in vitro and in vivo nerve regenerative effects. J Med Chem 2002, 45, 16, 3549.

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)	25354	methyl (2S)-2-piperidinecarboxylate		C₇H₁₃NO₂	详情	详情
(II)	26971	2-methoxy-2-oxoacetyl chloride	5781-53-3	C₃H₃ClO₃	详情	详情
(III)	60287	methyl 1-[2-(methyloxy)-2-oxoacetyl]-2-piperidinecarboxylate		C₁₀H₁₅NO₅	详情	详情
(IV)	60288	chloro(1,1-dimethylpropyl)magnesium		C₅H₁₁ClMg	详情	详情
(V)	60289	methyl 1-(3,3-dimethyl-2-oxopentanoyl)-2-piperidinecarboxylate		C₁₄H₂₃NO₄	详情	详情
(VI)	60290	1-(3,3-dimethyl-2-oxopentanoyl)-2-piperidinecarboxylic acid		C₁₃H₂₁NO₄	详情	详情

Extended Information