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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14628생성일: 2026년 10월 24일

Hydrochloric Acid → 1-(Tert-butoxycarbonylamino-methyl)-6,8-dimethoxy-isoquinoline-4-carboxylic acid

https://huagongshe.com/ko/reaction/14628

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcetateHCID 8857—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물1-(Tert-butoxycarbonylamino-methyl)-6,8-dimethoxy-isoquinoline-4-carboxylic acid ethyl esterHCID 59341080—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-(Tert-butoxycarbonylamino-methyl)-6,8-dimethoxy-isoquinoline-4-carboxylic acidHCID 5934109896%

반응 조건

온도50 °C

반응 단계

To a solution of 1-(tert-butoxycarbonylamino-methyl)-6,8-dimethoxy-isoquinoline-4-carboxylic acid ethyl ester (520 mg, 1.34 mmol) in THF (10 ml) and H2O (10 ml) under nitrogen, LiOH—H2O (95 mg, 2.3 mmol) was added. The reaction was stirred at 50° C. for 3.5 hours and at then at room temperature for 18 hours. EtOAc and water were then added and the pH was adjusted to 5 by dropwise addition of 6N HCl. The layers were then separated and the aqueous phase was extracted with EtOAc. The combined organic layers were then washed with brine, dried over magnesium sulfate and filtered. The solvent was removed under reduced pressure to give 1-(tert-butoxycarbonylamino-methyl)-6,8-dimethoxy-isoquinoline-4-carboxylic acid as a solid (464 mg, 96%). H1-NMR (DMSO): δ, 8.84 (s, 1H), 7.96 (s, 1H), 6.91 (t, 1H, J=5.4 Hz), 6.77 (s, 1H), 4.80 (d, 2H, J=5.43 Hz), 3.95 and 3.88 (s, 3H each), 1.36 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732446B1
출처 데이터셋uspto-grants-2010_06
ORD IDord-0ebda1cd5a5b46b19dc8d2e133fb3bbe
출처 메모uspto-grants-2010_06