Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 265316생성일: 2026년 10월 27일
Imidazole → 3-[(Tert-butyldimethylsilyloxy)methyl]-6-[methyloxy[3-hydroxyquinoxalin-2-yl]]-1,2-dithiin
https://huagongshe.com/reaction/265316
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Imidazole | HCID 795 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 반응물 | Diethyl azodicarboxylate | HCID 5462977 | — |
| 반응물 | 3-[(Tert-butyldimethylsilyloxy)methyl]-6-hydroxymethyl-1,2-dithiin | HCID 10062832 | — |
| 반응물 | 3-(Tert-butyldimethylsilyloxy)-2-hydroxyquinoxaline | HCID 178455110 | — |
| 반응물 | HCID 178517140 | HCID 178517140 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-[(Tert-butyldimethylsilyloxy)methyl]-6-[methyloxy[3-hydroxyquinoxalin-2-yl]]-1,2-dithiin | HCID 178488928 | 28.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05648354 |
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| 출처 데이터셋 | uspto-grants-1997_07 |
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| ORD ID | ord-7f775397e4964fcb85517dbb0ba849bd |
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| 출처 메모 | uspto-grants-1997_07 |
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