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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33753생성일: 2026년 10월 24일

Chloroform → HCID 44203175, 화합물

https://huagongshe.com/ko/reaction/33753

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물Acetic AnhydrideHCID 7918—
반응물Isoamyl NitriteHCID 8053—
반응물Potassium AcetateHCID 517044—
반응물Methyl 3-methylanthranilateHCID 2763406—
생성물HCID 44203175HCID 4420317568%

반응 단계

To a solution of the ester (17.5 g, 106 mmol) in chloroform (300 mL) was added acetic anhydride (22.6 mL, 239 mmol, 2.3 eq) while maintaining the temperature below 40° C. The reaction mixture was maintained at room temperature for 1 h when potassium acetate (3.00 g, 30.6 mmol, 0.3 eq) and isoamyl nitrite (30.6 mL, 228 mmol, 2.2 eqiv) was added. The reaction mixture was heated at reflux for 24 h and was allowed to cool to room temperature. The reaction mixture was washed with a saturated, aqueous solution of sodium bicarbonate, dried over sodium sulfate, and concentrated. Methanol (100 mL) and 6 N hydrochloric acid (100 mL) were added to the residue and the mixture was maintained for 18 h at rt. The volatiles were removed under reduced pressure and the residue was triturated with ethyl acetate (100 mL). The product was isolated by filteration, washed with ethyl acetate (20 mL), and dried to provide 15.3 g (68%) of methyl 1H-indazole-7-carboxylate hydrochloride. 1H NMR (500 MHz, DMSO-d6) δ 13.3 (bs, 1H), 8.26 (d, 1H), 8.12 (d, 1H), 8.25 (dd, 1H), 7.27 (t, 1H), 3.97 (s, 3H); MS (APCI) m/z 177 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429664B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-03713d90e522417b94e7a3e1e6e6d0f0
출처 메모uspto-grants-2008_09