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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2075769생성일: 2026년 10월 26일

Acetic Acid → HCID 178451867, 화합물

https://huagongshe.com/reaction/2075769

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물DiisopropylcarbodiimideHCID 12734—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물(2S)-1-((tert-butoxy)carbonyl)piperidine-2-carboxylic acidHCID 688617—
반응물2-[4-(4-Amino-phenylethynyl)-1H-pyrazol-3-yl]-4-chloro-phenolHCID 178507548—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물HCID 178451867HCID 17845186757.2%

반응 단계

To a solution of compound 24A (520 mg, 1.7 mmol) and N-Boc-2(S)-piperidinecarboxylic acid (8A) (584 mg, 2.55 mmol) in anhydrous dichloromethane (30 mL) was added N,N′-diisopropylcarbodiimide (DIPC, 0.4 mL, 2.55 mmol). The reaction mixture was stirred at rt overnight. The solvent was removed. To the residua were added THF (40 mL) and methanol (40 mL) and a solution of LiOH.H2O (2.0 g, 47.68 mmol) in water (20 mL). The mixture was stirred at rt for 3 h. It was then neutralized with acetic acid (3 mL, 52.41 mmol). The mixture was diluted with ethyl acetate (˜100 mL), washed with brine, and dried over sodium sulfate. It was filtered, concentrated and filtered again to remove diisopropylurea. The filtrate was purified with silica column chromatography eluting with hexanes/ethyl acetate (v/v 2/1, 3/2, 1/1) to provide the title compound (25A, 500 mg) as a yellowish solid in 57.2% yield. 1H NMR (CDCl3, 500 MHz) δ 10.62 (br s, 1H), 8.71 (d, 1H, J=2.0 Hz), 8.35 (br s, 1H), 7.84 (s, 1H), 7.55 (s, 4H), 7.22 (dd, 1H, J=9.0, 2.0 Hz), 6.99 (d, 1H, J=9.0 Hz), 4.90 (s, 1H), 4.05 (m, 1H), 2.90 (t, 1H, J=11.5 Hz), 2.35 (m, 1H), 1.80-1.30 (m, 16H). LCMS (ESI) m/z 587.15 (MNa+), 521.05 (MH+), 421.06; HPLC: tR=5.32 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07923004B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-9b8cbb0225dd473282649b4480a9deca
출처 메모uspto-grants-2011_04