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Methyl 2-oxo-1,2,3,4-tetrahydrothieno[3,2-b]pyrazine-6-carboxylate → Methyl 2-oxo-1,2-dihydrothieno[2,3-b]pyrazine-6-carboxylate

HRID 1184828
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HRID 1184828 반응식
[O:1]=[C:2]1[NH:7][C:6]2[CH:8]=[C:9]([C:11]([O:13][CH3:14])=[O:12])[S:10][C:5]=2[NH:4][CH2:3]1>C1COCC1.[O-2].[Mn+4].[O-2].[O-2].[Mn+2]>[O:1]=[C:2]1[NH:7][C:6]2[CH:8]=[C:9]([C:11]([O:13][CH3:14])=[O:12])[S:10][C:5]=2[N:4]=[CH:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 67125709Methyl 2-oxo-1,2,3,4-tetrahydrothieno[3,2-b]pyrazine-6-carboxylate

생성물 1

HCID 67125557Methyl 2-oxo-1,2-dihydrothieno[2,3-b]pyrazine-6-carboxylate수율 95%

시약·촉매·용매 3

HCID 160959Manganese oxide촉매HCID 178418406HCID 178418406, 화합물촉매HCID 8028Tetrahydrofuran용매

실험 절차

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To a suspension of methyl 2-oxo-1,2,3,4-tetrahydrothieno[3,2-b]pyrazine-6-carboxylate 20 (515 mg, 2.427 mmol) in THF (30 mL) was added manganese(IV) oxide (2.11 g, 24.27 mmol). The reaction was stirred at rt for 30 min. manganese oxide was filtrated and washed with EtOAc. The filtrate was evaporated to give crude methyl 2-oxo-1,2-dihydrothieno[3,2-b]pyrazine-6-carboxylate 21 (483 mg, 95%). NMR (400 MHz, DMSO-d6) 3.90 (s, 3H), 7.62 (br s, 1H), 8.13 (s, 1H), 12.80 (br s, 1H). (m/z)=211 (M+H)+.

후처리

  1. filtrationwas filtrated
  2. washwashed with EtOAc
  3. customThe filtrate was evaporated

출처 및 근거

ORD 기록
ord-a63983bbf26a4e568c3ebdfeef50c9dc
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08669256B2

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