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HRID 51354作成日:2026年10月27日

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

https://huagongshe.com/reaction/51354

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Ammonium HydroxideHCID 14923—
反応物9-[(Phenyl)methyl]-4-hydroxy-5-carbomethoxy carbazoleHCID 22337716—
溶媒MethanolHCID 887—
溶媒Ethyl AcetateHCID 8857—
生成物9-[(Phenyl)methyl]-4-hydroxy-5-carbamoyl carbazoleHCID 2233771826%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713645B1
出典データセットuspto-grants-2004_03
ORD IDord-60268cfd8da6451d99d15e8168b50feb
出典メモuspto-grants-2004_03