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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 589601생성일: 2026년 10월 25일

Sodium hydride → HCID 71625636, 화합물

https://huagongshe.com/reaction/589601

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1H-Indole, 6-methyl-HCID 137928—
반응물Pyridine-2-sulfonyl ChlorideHCID 3787675—
용매TetrahydrofuranHCID 8028—
생성물HCID 71625636HCID 7162563657.7%

반응 단계

6-Methylindole (42) (7.34 g, 56.0 mmol) was added in portions to a mixture of sodium hydride (3.36 g, 84.0 mmol) in THF (80 mL) at 0° C. After 15 min, pyridine-2-sulfonyl chloride (43) (10.0 g, 56.0 mmol) was added, and the reaction was allowed to warm to rt and stirred overnight under N2. The reaction mixture was then quenched with ice water and extracted with EtOAc. The organic layers were combined, dried over MgSO4, and concentrated in vacuo. The crude product was purified by flash column chromatography eluting with a linear gradient ranging from 0 to 40% EtOAc-hexanes to provide 8.8 g (57%) of product 44 as a brown gum. 1H NMR (300 MHz, CDCl3) δ 2.44 (s, 3H), 6.62 (dd, J=1, 4 Hz, 1H), 7.03-7.06 (m, 1H), 7.41 (d, J=8 Hz, 1H), 7.41-7.45 (m, 1H), 7.59 (d, J=4 Hz, 1H), 7.79-7.81 (m, 1H), 7.84-7.90 (m, 1H), 8.10 (dt, J=1, 8 Hz, 1H), 8.58-8.60 (m, 1H). LC-MS (CI): m/z 273.0 [(M+H)+ C14H12N2O2S requires 272.06].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09233921B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-bf1088f376d1480fbf73035e44118c5d
출처 메모uspto-grants-2016_01