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HRID 248434생성일: 2026년 10월 26일

Hydrochloric Acid → 3-(6-chloro-1H-indol-3-yl)-2-oxopropanoic acid

https://huagongshe.com/reaction/248434

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물MethanolHCID 887—
반응물TriethylamineHCID 8471—
반응물6-ChlorotryptophanHCID 65259—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
촉매ZincchlorideHCID 3007855—
생성물3-(6-chloro-1H-indol-3-yl)-2-oxopropanoic acidHCID 979471754%

반응 단계

To 600 mg of 6-chloro-DL-tryptophan, suspended in 5 ml of methanol, are added, at room temperature, 0,230 ml of triethylamine and the mixture is stirred for approximately 10 minutes. Then, rapidly and under stirring, pyridine-4-carboxyaldehyde (0,240 ml) is added. After approximately 5 minutes, total dissolution of the suspension is obtained. Stirring is continued for 10 minutes. 122 mg of anhydrous ZnCl2 are then added, stirred for 10 minutes, followed by 0,490 ml of 1,8-diazabicyclo-(5,4,0)-undec-7-ene. The solution becomes orange-red in colour. It is left under stirring for approximately 80-90 minutes at room temperature. The limpid red solution is then quickly added dropwise and under rapid stirring to 100 ml of HCl 1N preheated to 50° C. After approximately 10 minutes from completion of the addition a spontaneous precipitation occurs, increasing in time, of a yellowish solid. The mixture is left for a further 20 minutes at 55° C., then for approximately 3 hours it is cooled to room temperature. The abundant precipitate is filtered, washed with acidic water and dried. 195 mg are recovered, with a yield of 54%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210215
출처 데이터셋uspto-grants-1993_05
ORD IDord-001e6f96773640589f57149156f64e64
출처 메모uspto-grants-1993_05