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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384553생성일: 2026년 10월 25일

Citric Acid → 3-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl]-5-Methylhexanoic Acid

https://huagongshe.com/reaction/384553

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참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물ChlorotrimethylsilaneHCID 6397—
반응물TriethylamineHCID 8471—
반응물PregabalinHCID 5486971—
반응물HCID 66753307HCID 66753307—
용매DichloromethaneHCID 6344—
생성물3-{[(alpha-Isobutanoyloxyethoxy)carbonyl]aminomethyl]-5-Methylhexanoic AcidHCID 1605923448%

반응 조건

온도0 °C

반응 단계

To a stirred suspension of pregabalin (2) (150 mg, 0.94 mmol) in anhydrous dichloromethane (10 mL) at 0° C. was added triethylamine (0.26 mL, 1.88 mmol) and trimethylchlorosilane (0.24 mL, 1.88 mmol). After stirring for 15 min at 0° C., a solution of α-isobutanoyloxyethyl-p-nitrophenyl carbonate (111) (267 mg, 0.94 mmol) in dichloromethane (3 mL) was added. The resulting mixture was stirred at room temperature for 1.5 h. The reaction mixture was acidified with citric acid and extracted with dichloromethane. The combined organic extracts were washed with brine and dried over Na2SO4. After filtration and evaporation, the crude product was purified by silica gel chromatography, eluting first with dichloromethane to remove nitrophenol, then with 30% ethyl acetate in dichloromethane to afford 130 mg (48%) of the title compound as a mixture of two diastereomers. 1H-NMR (CDCl3, 400 MHz): δ 0.90 (m, 6H), 1.70 (m, 8H), 1.46 (d, J=5.6 Hz, 3H), 1.66 (1H, m), 2.15 (m, 1H), 2.33 (m, 2H), 2.53 (m, 1H), 3.12 (m, 1H), 3.29 (m, 1H), 5.08 (t, J=6.0 Hz, 1H), 6.79 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367722B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-a889676cb49e412cba9ab6a090bcc92a
출처 메모uspto-grants-2013_02