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HRID 1486689作成日:2026年10月25日

Acetic Acid → 1-(3-tert-Butoxycarbonylamino-benzyl)-piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1486689

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Ethyl 4-piperidinecarboxylateHCID 70770—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物3-(BOC-Amino)benzaldehydeHCID 16740736—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物1-(3-tert-Butoxycarbonylamino-benzyl)-piperidine-4-carboxylic acid ethyl esterHCID 86706521—

反応手順

A mixture of (3-formyl-phenyl)-carbamic acid tert-butyl ester (Schadendorf T et al., Tetrahedron Letters (2007), 48(51), 9044-9047), (1 g, 4.52 mmol), ethyl isonipecotate (800 mg, 5.09 mmol) and TEA (0.7 mL, 5 mmol) in MeOH (50 mL) is treated with acetic acid (1.03 mL, 18 mmol) and stirred at RT for 2 h. Sodium cyanoborohydride (398 mg, 6.33 mmol) is added at once and the reaction mixture is stirred for 18 h at RT. Water (5 mL) is added to the mixture and the solvents are evaporated. The residue is partitioned between diethyl ether (50 mL) and aqueous 0.1N HCl (50 mL). The aqueous phase is separated, washed twice with diethyl ether (25 mL) and basified with 1N NaOH solution (10 mL). The aqueous phase is extracted three times with DCM (3×50 mL). The combined organic phases are dried over MgSO4 and evaporated. The title compound is obtained as a thick oil; LC-MS A: tR=0.71 min; [M+H]+=363.48.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09428456B2
出典データセットuspto-grants-2016_08
ORD IDord-d53e229b4f10439d9d01db4433951973
出典メモuspto-grants-2016_08