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HRID 265316생성일: 2026년 10월 27일

Imidazole → 3-[(Tert-butyldimethylsilyloxy)methyl]-6-[methyloxy[3-hydroxyquinoxalin-2-yl]]-1,2-dithiin

https://huagongshe.com/reaction/265316

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참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물TriphenylphosphineHCID 11776—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물3-[(Tert-butyldimethylsilyloxy)methyl]-6-hydroxymethyl-1,2-dithiinHCID 10062832—
반응물3-(Tert-butyldimethylsilyloxy)-2-hydroxyquinoxalineHCID 178455110—
반응물HCID 178517140HCID 178517140—
용매TetrahydrofuranHCID 8028—
생성물3-[(Tert-butyldimethylsilyloxy)methyl]-6-[methyloxy[3-hydroxyquinoxalin-2-yl]]-1,2-dithiinHCID 17848892828.2%

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온도0 °C

반응 단계

To a stirred solution of 3-(hydroxymethyl)-6-[(tert-butyldimethylsilyloxy)methyl]-1,2-dithiin (U.S. Ser. No. 08/212,096) (200 mg, 0.688 mmol) of in 2 mL dry THF was added a solution of 3-(tert-butyldimethylsilyloxy)-2-hydroxyquinoxaline obtained from the reaction of 2,3-dihydroxyquinoxaline with tert-butyldimethylsilyl chloride and imidazole as in Example 6 (248 mg, 1.753 mmol) in 2 mL THF, followed by addition of triphenylphosphine (220 mg, 0.839 mmol). The resulting solution was cooled to 0° C., then 140 μL (155 mg, 0.890 mmol) of diethylazodicarboxylate was added, and the reaction mixture was kept at 0°-5° C. for 2 h until TLC analysis showed the reaction to be complete. For isolation of the products, the reaction mixture poured directly onto a silica gel column and eluted with ethyl acetate-hexane, 1:6, to give 3-[(tert-butyldimethylsilyloxy)methyl]-6-[methyloxy[3-hydroxyquinoxalin-2-yl]]-1,2-dithiin (104 mg, 28.2%). No product of N-alkylation was isolated; MS (+LSIMS) 549.4 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05648354
출처 데이터셋uspto-grants-1997_07
ORD IDord-7f775397e4964fcb85517dbb0ba849bd
출처 메모uspto-grants-1997_07