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Dimethylamine, hydrochloride → 8-acetyl-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide

HRID 1947355
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HRID 1947355 반응식
[CH2:1]([N:3](C(C)C)[CH:4](C)C)C.[C:10]([C:13]1[CH:14]=[C:15]([C:30]([OH:32])=O)[CH:16]=[C:17]2[C:22]=1[O:21][C:20]([N:23]1[CH2:28][CH2:27][O:26][CH2:25][CH2:24]1)=[CH:19][C:18]2=[O:29])(=[O:12])[CH3:11].Cl.CNC>C(Cl)Cl>[C:10]([C:13]1[CH:14]=[C:15]([C:30]([N:3]([CH3:4])[CH3:1])=[O:32])[CH:16]=[C:17]2[C:22]=1[O:21][C:20]([N:23]1[CH2:28][CH2:27][O:26][CH2:25][CH2:24]1)=[CH:19][C:18]2=[O:29])(=[O:12])[CH3:11]
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참가 물질

5

반응물 3

HCID 10473Dimethylamine, hydrochlorideHCID 81531DiisopropylethylamineHCID 582349818-acetyl-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid

생성물 1

HCID 582350348-acetyl-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide수율 46%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

N-ethyl-N-isopropylpropan-2-amine (9.4 mL, 53.9 mmol) was added to 8-acetyl-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid (5.7 g, 18 mmol) in DCM (100 mL). Five minutes later dimethylamine hydrochloride (2.9 g, 35.9 mmol) and 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborate (6.92 g, 21.6 mmol) were added. The mixture was diluted with DCM, washed with NaHCO3, dried over magnesium sulfate and concentrated to afford the crude product which was purified by flash chromatography on silica gel eluting with 0 to 5% MeOH/DCM. The solvent was evaporated to dryness to afford 8-acetyl-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide (2.75 g, 46%) as a yellow solid. Mass Spectrum: M+H+ 345.

후처리

  1. washwashed with NaHCO3
  2. dry with materialdried over magnesium sulfate
  3. concentrationconcentrated
  4. customto afford the crude product which
  5. customwas purified by flash chromatography on silica gel eluting with 0 to 5% MeOH/DCM
  6. customThe solvent was evaporated to dryness

출처 및 근거

ORD 기록
ord-a3295f4939ef44a887728d7a01e5a6eb
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399460B2

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