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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2355359생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2355359

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물rel-(1R,3S)-3-Benzoylcyclohexanecarboxylic acidHCID 11345291—
반응물(S)-2-(trimethylsilyl)ethyl 2-amino-3-cyclohexylpropylcarbamateHCID 59382944—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-(trimethylsilyl)ethyl (S)-2-(3-benzoylcyclohexanecarboxamido)-3-cyclohexylpropylmethylcarbamateHCID 6719172594.6%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07754737B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-b4655aa62cbc49b6b9a3a97be4652fa6
출처 메모uspto-grants-2010_07