戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 28352作成日:2026年10月23日

Water → 2,5,6-Trichloro-3-[N-(methoxycarbonylamino)iminomethylidene]-1-(beta-D-ribofuranosyl)indole

https://huagongshe.com/ja/reaction/28352

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl carbazateHCID 80519—
反応物FtcriHCID 3011610—
溶媒MethanolHCID 887—
生成物2,5,6-Trichloro-3-[N-(methoxycarbonylamino)iminomethylidene]-1-(beta-D-ribofuranosyl)indoleHCID 8659897085%

反応手順

2,5,6-Trichloro-3-formyl-1-(β-D-ribofuranosyl)indole (4.3, 122 mg, 0.32 mmol) was dissolved in MeOH (10 mL) to which was added methyl hydrazinocarboxylate (115 mg, 1.3 mmol). The resulting solution was heated on a 60 C oil bath for 16 h, then cooled to room temperature and poured into 100 mL of water, and the solvent evaporated to approx 50 mL. The resulting suspension was cooled to 4C, then filtered and the solids rinsed with cold water (25 mL). The solids were recrystallized from boiling EtOAc/hexane to yield 123 mg (85%) of 4.31 as a pale pink crystalline solid: mp 217-219 C; Rf 0.2 (10% MeOH/CHCl3); 1H-NMR (500 MHz, DMSO-d6): δ 11.17 (b, 1H, D2O exch.), 8.54 (s, 1H), 8.42 (s, 1H), 8.22 (b, 1H), 5.92 (d, 1H), 5.42-5.37 (m, 2H, D2O exch.), 5.25 (d, 1H, D2O exch.), 4.43 (q, 1H), 4.15 (d, 1H), 3.98 (d, 1H), 3.72 (b, 5H). 13C-NMR (125 MHz, DMSO-d6): δ 153.88, 133.17, 129.33, 126.08, 124.96, 124.06, 122.17, 115.34, 108.59, 88.76, 86.03, 71.30, 69.73, 69.62, 61.07, 52.04. HRMS (ES) m/z calcd. for C16H16Cl3N3O6·Na 474.0002, found 473.9999. Anal calcd for C16H16Cl3N3O6·¼H2O: C, 42.03; H, 3.64; N, 9.19. Found: C, 42.11; H, 3.92; N, 9.18.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419963B2
出典データセットuspto-grants-2008_09
ORD IDord-723df91f03f94b6992372177f3519484
出典メモuspto-grants-2008_09