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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 401604생성일: 2026년 10월 25일

Acetic Acid → 7-Fluorotryptophan

https://huagongshe.com/reaction/401604

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium HydroxideHCID 14798—
반응물2-(7-Fluoro-1H-indol-3-ylmethyl)-2-formylamino-malonic acid diethyl esterHCID 57563301—
용매TetrahydrofuranHCID 8028—
생성물7-FluorotryptophanHCID 1593014852%

반응 단계

A solution of 2-(7-Fluoro-1H-indol-3-ylmethyl)-2-formylamino-malonic acid diethyl ester in THF was treated with NaOH (300 mg in 10 mL water) at room temperature for 24 hr. The mixture was slowly acidified with acetic acid (5 mL) and then refluxed for 24 hr. The reaction mixture was concentrated under vacuum, and treated with dil. HCl (10 mL, 3M) and then again refluxed for ˜16 h. The reaction was allowed to cool to room temperature. The pH was adjusted to 6.0 with 2M KOH. The white solid that formed was filtered, washed with water, and dried under vacuum to give 7-fluoro-tryptophan (282 mg, 52%): mp 256-261° C., 1H NMR (500 MHz, DMSO-d6): 2.92-2.97 (dd, J=8.5 and 15 Hz, 1H), 3.25-3.29 (dd, J=4.0 and 15 Hz, 1H), 3.38-3.41 (dd, J=4.0 and 8.5 Hz, 1H), 6.87-6.96 (m, 2H), 7.25 (s, 1H), 7.37 (d, J=7.5 Hz, 1H), 11.36 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741942B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-00bd0c5c0620447892c414d223ac490b
출처 메모uspto-grants-2014_06