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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 724701생성일: 2026년 10월 25일

Triethylsilane → Methyl 2-[4-([4-(1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)benzyl]oxymethyl)phenoxy]-6-methoxybenzoate

https://huagongshe.com/reaction/724701

반응식

참여 물질

역할이름HCID투입량
반응물TriethylsilaneHCID 12052—
반응물5-[4-(Hydroxymethyl)phenyl]isothiazol-3(2H)-one 1,1-dioxideHCID 21878837—
반응물Methyl 2-(4-formylphenoxy)-6-methoxybenzoateHCID 21879099—
용매Hydrochloric AcidHCID 313—
용매1,4-DioxaneHCID 31275—
생성물Methyl 2-[4-([4-(1,1-dioxido-3-oxo-2,3-dihydroisothiazol-5-yl)benzyl]oxymethyl)phenoxy]-6-methoxybenzoateHCID 587466056%

반응 단계

Methyl 2-(4-formylphenoxy)-6-methoxybenzoate (0.071 g, 0.24 mmol) and 5-[4-(hydroxymethyl)phenyl]isothiazol-3(2H)-one 1,1-dioxide (0.050 g, 0.21 mmol) were dissolved in 4 M hydrogen chloride in 1,4-dioxane (2.1 m). The reaction was stirred at ambient temperature for 1.25 h. Triethylsilane (0.13 mL, 0.84 mmol) was added and stirred for 18 h. The reaction was quenched with acetone and evaporated. The product was purified on a 50 mm Luna C18 column using a 20–100% acetonitrile in water gradient with 0.05% trifluoroacetic acid at 30 mL per minute over a 30 minute period. The product was lyophilized to give a white powder (6 mg, 6%). 1H NMR (400 MHz, CDCl3): δ 7.79 (d, J=8.4 Hz, 2H), 7.53 (d, J=8.1 Hz, 2H), 7.32 (m, 2H), 6.71 (s, 1H), 6.69 (d, J=8.5 Hz, 1H), 6.49 (d, J=8.3 Hz, 1H), 4.62 (m, 2H), 4.55 (m, 2H), 3.87 (s, 3H), 3.85 (s, 3H); LCMS found for C26H23NNaO8S (M+Na)+: m/z=532.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141596B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-114ff7770eb54feca447758c34f78314
출처 메모uspto-grants-2006_11