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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1922243생성일: 2026년 10월 26일

1,4-Dioxane → (S)-6-(2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yloxy)-N-(piperidin-3-yl)benzo[d]thiazol-2-amine

https://huagongshe.com/reaction/1922243

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물(S)-tert-butyl 3-(6-(2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yloxy)benzo[d]thiazol-2-ylamino)piperidine-1-carboxylateHCID 57725561—
용매Hydrochloric AcidHCID 313—
생성물(S)-6-(2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yloxy)-N-(piperidin-3-yl)benzo[d]thiazol-2-amineHCID 5772557194.7%

반응 단계

(S)-tert-butyl 3-(6-(2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yloxy)benzo[d]thiazol-2-ylamino)piperidine-1-carboxylate (9.6 mg, 19 μmol) was dissolved in 1 ml of 4M HCl in dioxane (4 mmol). The reaction solution was stirred at room temperature for 1 hour. The crude reaction solution was evaporated in vacuo to give (S)-6-(2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yloxy)-N-(piperidin-3-yl)benzo[d]thiazol-2-amine (7.6 mg, 18 μmol) as white solid. ES/MS m/z 407.1 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08173689B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-892162a79d814bd982e9b00c2a23f75f
출처 메모uspto-grants-2012_05