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HRID 2355359作成日:2026年10月25日

Diisopropylethylamine → 2-(trimethylsilyl)ethyl (S)-2-(3-benzoylcyclohexanecarboxamido)-3-cyclohexylpropylmethylcarbamate

https://huagongshe.com/reaction/2355359

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物rel-(1R,3S)-3-Benzoylcyclohexanecarboxylic acidHCID 11345291—
反応物(S)-2-(trimethylsilyl)ethyl 2-amino-3-cyclohexylpropylcarbamateHCID 59382944—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物2-(trimethylsilyl)ethyl (S)-2-(3-benzoylcyclohexanecarboxamido)-3-cyclohexylpropylmethylcarbamateHCID 6719172594.6%

反応手順

To a stirred solution of cis-3-benzoylcyclohexane-1-carboxylic acid (78 mg, 0.34 mmol), 2-(trimethylsilyl)ethyl (S)-2-amino-3-cyclohexylpropylcarbamate (116 mg, 0.37 mmol) and diisopropylethylamine (0.13 mL, 0.70 mmol) in CH2Cl2 (2 mL) were added solid 2-(7-aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU, 200 mg, 0.53 mmol) and DMF (0.5 mL). The mixture was stirred at rt for 3 h, diluted with ether (90 mL), washed with 5% aqueous HCl (25 mL), sat'd aqueous NaHCO3 (25 mL), and brine (25 mL) and dried over Na2SO4. Removal of the solvent under reduced pressure left an oil (260 mg) which was applied to a 2-g silica SPE cartridge and eluted sequentially with 0, 10, 25, 50, 75, and 100% EtOAc in hexanes (15 mL of each) to give six fractions. Fractions 2-4 were pooled and evaporated to afford 2-(trimethylsilyl)ethyl (S)-2-(3-benzoylcyclohexane-carboxamido)-3-cyclohexylpropylmethylcarbamate (170 mg, 91%) as an oil. MS ESI+ve m/z 528 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07754737B2
出典データセットuspto-grants-2010_07
ORD IDord-b4655aa62cbc49b6b9a3a97be4652fa6
出典メモuspto-grants-2010_07