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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 298생성일: 2026년 10월 23일

Methylamine → N-Methyl-6-nitrobenzo[D]thiazol-2-amine

https://huagongshe.com/ko/reaction/298

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참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물2-Bromo-6-nitrobenzothiazoleHCID 11623040—
시약Cesium carbonateHCID 10796—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Palladium (II) acetateHCID 4144353—
용매1,4-DioxaneHCID 31275—
생성물N-Methyl-6-nitrobenzo[D]thiazol-2-amineHCID 6385686.19%

반응 조건

온도150 °C

반응 단계

methanamine (0.793 mL, 19.30 mmol), 2-bromo-6-nitrobenzo[d]thiazole (1 g, 3.86 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (0.268 g, 0.46 mmol), cesium carbonate (1.886 g, 5.79 mmol) and diacetoxypalladium (0.043 g, 0.19 mmol) were suspended in 1,4-dioxane (8 mL) and sealed into a microwave tube. The reaction was heated to 150°C for 30 minutes in the microwave reactor and cooled to RT. The crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and pure fractions were evaporated to dryness to afford a crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 50% DCM in EtOAc. Pure fractions were evaporated to dryness to afford N-methyl-6-nitrobenzo[d]thiazol-2-amine (0.050 g, 6.19 %) as a yellow solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-ced8329d85d843b9adb25a3a7cf2fe09
출처 메모750 AstraZeneca ELN dataset