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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65072생성일: 2026년 10월 25일

Methyl iodide → Methyl (1S, 3S)-3-hydroxymethyl-1-methyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioate

https://huagongshe.com/reaction/65072

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Carbon DisulfideHCID 6348—
반응물TriethylamineHCID 8471—
반응물(1S, 3S)-3-hydroxymethyl-1-methyl-1,2,3,4-tetrahydro-beta-carbolineHCID 13375562—
용매Dimethyl SulfoxideHCID 679—
생성물Methyl (1S, 3S)-3-hydroxymethyl-1-methyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioateHCID 1337553090%

반응 단계

(1RS, 3RS)-cis-3-Hydroxymethyl-1-methyl-1,2,3,4-tetrahydro-β-carboline (4.326 g) is dissolved in dimethylsulfoxide (20 ml), and thereto are added CS2 (2.4 ml) and triethylamine (5.6 ml). The mixture is stirred at room temperature for 30 minutes, and thereto is added dropwise methyl iodide (2.5 ml), and the mixture is stirred at room temperature for 2 hours. The reaction mixture is poured onto ice-water, and the mixture is extracted with ethyl acetate. The extract is washed with water, 5% HCl and water in order, dried over sodium sulfate and then distilled to remove the solvent. The residue is recrystallized from aqueous ethanol to give the title compound (5.5 g, 90%) as colorless needles, m.p. 164°-166° C., NMR (CDCl3, δ): 1.68 (d, J=6.8 Hz, 3H, C1 --CH3), 2.73 (s, 3H, CSSCH3); Mass m/e: 306 (M+), 258 (M+ --CH 3 SH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04612317
출처 데이터셋uspto-grants-1986_09
ORD IDord-332c494c01eb42aa973a21aa6f49dcd1
출처 메모uspto-grants-1986_09