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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51354생성일: 2026년 10월 26일

Hydrochloric Acid → 9-[(Phenyl)methyl]-4-hydroxy-5-carbamoyl carbazole

https://huagongshe.com/reaction/51354

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ammonium HydroxideHCID 14923—
반응물9-[(Phenyl)methyl]-4-hydroxy-5-carbomethoxy carbazoleHCID 22337716—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물9-[(Phenyl)methyl]-4-hydroxy-5-carbamoyl carbazoleHCID 2233771826%

반응 단계

A solution of the 9-[(phenyl)methyl]-4-hydroxy-5-carbomethoxy carbazole (200 mg, 0.6 mM) in 4 mL MeOH and 40 mL concentrated aqueous ammonium hydroxide was sonicated for 30 h at 40-50° C. The mixture was diluted with ethyl acetate and acidified to pH 1 with 5 N HCl. The aqueous layer was extracted three times with ethyl acetate. The combined organic extracts were washed with saturated brine, dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (elution with gradient methylene chloride/ethyl acetate) to afford 50 mg (26%) of the 9-[(phenyl)methyl]-4-hydroxy-5-carbamoyl carbazole as a white solid. 1H NMR (DMSO-d6) δ10.5 (s, 1H), 8.8 (br s, 1H), 8.4 (br s, 1H), 7.85 (dd, 1H, J=1 and 8 Hz), 7.5-7.1 (m, 9H), 6.6 (d, 1H, J=8 Hz), and 5.8 (s, 2H). IR (KBr, cm−1) 3428, 3198, 3063, 1631, 1599, 1579, 1562, 1496, 1442, 1330, 1261, 1215, 775, and 697. MS (ES) m/e 315, 317.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713645B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-60268cfd8da6451d99d15e8168b50feb
출처 메모uspto-grants-2004_03