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【结 构 式】

【分子编号】48169

【品名】10-undecenoyl chloride

【CA登记号】38460-95-6

【 分 子 式 】C11H19ClO

【 分 子 量 】202.72396

【元素组成】C 65.17% H 9.45% Cl 17.49% O 7.89%

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 title compound was prepared by two related procedures. The acylation of L-glutamine (I) with 10-undecenoyl chloride (II) under Schotten-Baumann conditions afforded N-undecenoylglutamine (III). This was then cyclized to the title glutarimide derivative by treatment with dicyclohexylcarbodiimide and N-hydroxysuccinimide.

1 Fox, D.J.; Grainger, D.J.; Reckless, J.; Warren, S.G.; Design, synthesis, and preliminary pharmacological evaluation of N-acyl-3-aminoglutarimides as broad-spectrum chemokine inhibitors in vitro and anti-inflammatory agents in vivo. J Med Chem 2002, 45, 2, 360.
2 Grainger, D.J.; Tatalick, L.M. (NeoRx Corp.); Cpds. and methods to inhibit or augment an inflammatory response. WO 0042071 .
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) 24948 L-glutamine 56-85-9 C5H10N2O3 详情 详情
(II) 48169 10-undecenoyl chloride 38460-95-6 C11H19ClO 详情 详情
(III) 48170 (2S)-5-amino-5-oxo-2-(10-undecenoylamino)pentanoic acid C16H28N2O4 详情 详情
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