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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1497028생성일: 2026년 10월 25일

Diisopropylcarbodiimide → HCID 178453874, 화합물

https://huagongshe.com/reaction/1497028

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물3,4-Dichloro-N'-hydroxybenzene-1-carboximidamideHCID 11264185—
반응물HCID 178453971HCID 178453971—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매PyridineHCID 1049—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물HCID 178453874HCID 17845387457.9%

반응 단계

A microwave vial was charged with cis-4-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid (0.24 g, 0.98 mmol), DMAP (0.12 g, 0.98 mmol) and Intermediate 33A (0.20 g, 0.98 mmol). The reactants were dissolved in DMF (1 mL) and DIC (0.15 mL, 0.98 mmol) was added. The reaction mixture was stirred at rt for 14 h. The reaction mixture was diluted in 3 mL of pyridine. The vial was capped and the reaction mixture was heated in the microwave at 145° C. for 20 minutes, allowed to cool to rt, diluted with EtOAc and washed with water and brine. The solution were concentrated under reduced pressure and purified by flash chromatography with EtOAc/hexanes to give Intermediate 33B (233 mg, 0.565 mmol, 57.9% yield) as a white solid. LCMS=434.1 [M+1], RT=2.43 min (Method B); 1H NMR (500 MHz, chloroform-d) δ ppm 8.19 (1H, d, J=1.93 Hz), 7.92 (1H, dd, J=8.53, 1.93 Hz), 7.56 (1H, d, J=8.25 Hz), 4.59 (1H, br. s.), 3.71 (1H, d, J=9.63 Hz), 3.14-3.22 (1H, m), 2.07-2.17 (2H, m), 1.92-2.02 (2H, m), 1.84 (2H, td, J=8.67, 4.13 Hz), 1.62-1.73 (2H, m), 1.44 (9H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09199946B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-1e1a5803fc7a49bb97c0f57f7e6e582b
출처 메모uspto-grants-2015_12