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HRID 552206생성일: 2026년 10월 26일

Methane → 6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-beta-carbolin-8-ylamine

https://huagongshe.com/reaction/552206

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물Ammonium ChlorideHCID 25517—
반응물[2-(6-chloro-8-nitro-9H-beta-carbolin-7-ylsulfanyl)-ethyl]-dimethyl-amineHCID 67166181—
촉매IronHCID 23925—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
생성물6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-beta-carbolin-8-ylamineHCID 67164517107%

반응 조건

온도60 °C

반응 단계

A 50 ml round-bottom flask with a magnetic stirrer was charged with [2-(6-chloro-8-nitro-9H-β-carbolin-7-ylsulfanyl)-ethyl]-dimethyl-amine (106 mg, 0.30 mmol) in 8 ml of anhydrous ethanol. To the resulting orange mixture at RT was added 0.33 M aqueous ammonium chloride (1.95 ml, 0.64 mmol) and iron powder (540 mg, 9.67 mmol). The reaction mixture was heated to 60° C. and stirred vigorously for 20 hr. Next, the mixture was cooled to RT, diluted with ethyl acetate (20 ml) and activated charcoal (ca. 150 mg) was added. The resulting mixture was filtered through a pad of celite and the resulting filtrate concentrated to afford 103 mg of 6-chloro-7-(2-dimethylamino-ethylsulfanyl)-9H-β-carbolin-8-ylamine as a yellow solid. The crude product was used directly in the coupling step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951801B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-867bd3fb01d946509767c125250c1e0f
출처 메모uspto-grants-2011_05