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2-Methoxyethylamine → Methyl 4,7-dihydro-5-(2-methoxyethyl)amino-4,7-dioxobenzo[b]thiophene-2-carboxylate

HRID 1582185
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반응식

HRID 1582185 반응식
[CH3:1][O:2][CH2:3][CH2:4][NH2:5].[O:6]=[C:7]1[C:15]2[CH:14]=[C:13]([C:16]([O:18][CH3:19])=[O:17])[S:12][C:11]=2[C:10](=[O:20])[CH:9]=[CH:8]1>O1CCCC1>[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:8]1[C:7](=[O:6])[C:15]2[CH:14]=[C:13]([C:16]([O:18][CH3:19])=[O:17])[S:12][C:11]=2[C:10](=[O:20])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 80182-MethoxyethylamineHCID 507039Methyl 4,7-dioxobenzothiophene-2-carboxylate

생성물 1

HCID 12987499Methyl 4,7-dihydro-5-(2-methoxyethyl)amino-4,7-dioxobenzo[b]thiophene-2-carboxylate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

2-Methoxyethylamine (1.6 ml) was added to a solution of methyl 4,7-dihydro-4,7-dioxobenzo[b]thiophene-2-carboxylate (2.4 g) in tetrahydrofuran (100 ml) and the mixture was stirred at room temperature for 27 hours. After evaporation of the solvent, the residue was purified by silica gel column chromatography (elution with chloroform) to give methyl 4,7-dihydro-5-(2-methoxyethyl)amino-4,7-dioxobenzo[b]thiophene-2-carboxylate (1.5 g) as a yellow powder.

후처리

  1. customAfter evaporation of the solvent
  2. customthe residue was purified by silica gel column chromatography (elution with chloroform)

출처 및 근거

ORD 기록
ord-2e37fe5b0f2046879bc553a1533a4612
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06734203B2

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