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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80659생성일: 2026년 10월 23일

1-Butanesulfonyl chloride → 5-((2-(1-(Butylsulfonyl)piperidin-4-yl)-2H-1,2,3-triazol-4-yl)methoxy)-2-(1H-tetrazol-1-yl)pyridine

https://huagongshe.com/ko/reaction/80659

반응식

참여 물질

역할이름HCID투입량
반응물1-Butanesulfonyl chlorideHCID 75430—
반응물5-((2-(piperidin-4-yl)-2H-1,2,3-triazol-4-yl)methoxy)-2-(1H-tetrazol-1-yl)pyridine hydrochlorideHCID 68746624—
생성물5-((2-(1-(Butylsulfonyl)piperidin-4-yl)-2H-1,2,3-triazol-4-yl)methoxy)-2-(1H-tetrazol-1-yl)pyridineHCID 25174426—

반응 단계

The title compound was synthesized using Intermediate 15 and 1-butanesulfonyl chloride in a similar manner as described in Example 39. 1H NMR (DMSO-d6): δ 10.08 (1H, s), 8.41 (1H, d), 8.00 (1H, d), 7.96 (1H, s), 7.86 (1H, dd), 5.36 (2H, s), 4.71 (1H, m), 3.63 (2H, m), 3.01 (4H, m), 2.2 (2H, m), 1.99 (2H, m), 1.64 (2H, m), 1.39 (2H, m), 0.89 (3H, t).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846675B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b6926748903643e48749f99345296122
출처 메모uspto-grants-2014_09