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Morpholine → HCID 58356387, 화합물

HRID 244612
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HRID 244612 반응식
[CH:1]([C:3]1[S:4][C:5]([CH:13]([CH3:15])[CH3:14])=[C:6]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[N:7]=1)=O.[NH:16]1[CH2:21][CH2:20][O:19][CH2:18][CH2:17]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)(O)[O-].[Na+]>C(Cl)Cl>[CH3:14][CH:13]([C:5]1[S:4][C:3]([CH2:1][N:16]2[CH2:21][CH2:20][O:19][CH2:18][CH2:17]2)=[N:7][C:6]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8083MorpholineHCID 516892Sodium BicarbonateHCID 5049666Sodium triacetoxyborohydrideHCID 58356391HCID 58356391, 화합물

생성물 1

HCID 58356387HCID 58356387, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Ethyl 2-formyl-5-(1-methylethyl)-1,3-thiazole-4-carboxylate (150 mg) was dissolved in anhydrous DCM (10 ml) and morpholine (0.064 ml) was added and the mixture stirred under nitrogen for 2 h at RT. Sodium triacetoxyborohydride (280 mg) was added and the mixture stirred at RT for 18 h. Sodium bicarbonate (20 ml) and DCM (20 ml) were added and separated by hydrophobic frit. The solvent was removed in vacuo and purified by column chromatography on silica gel (10 g silica), eluting with a gradient of 0-100% ethyl acetate in cyclohexane to give the title compound as a yellow oil (77 mg).

후처리

  1. stirringthe mixture stirred at RT for 18 h
  2. customseparated by hydrophobic frit
  3. customThe solvent was removed in vacuo
  4. custompurified by column chromatography on silica gel (10 g silica)
  5. washeluting with a gradient of 0-100% ethyl acetate in cyclohexane

출처 및 근거

ORD 기록
ord-06c0d69e06884b71b66f66017d69e0dd
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658635B2

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