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Water → 4-(6-Chloro-2-oxo-2H-1-benzopyran-4-yl)-butyramide

HRID 495152
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HRID 495152 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][C:9](=[O:11])[CH:8]=[C:7]([CH2:12][CH2:13][CH2:14][C:15]#[N:16])[C:6]=2[CH:17]=1.[OH2:18]>OS(O)(=O)=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][C:9](=[O:11])[CH:8]=[C:7]([CH2:12][CH2:13][CH2:14][C:15]([NH2:16])=[O:18])[C:6]=2[CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 962WaterHCID 118174844-(6-Chloro-2-oxo-2H-1-benzopyran-4-yl)-butyronitrile

생성물 1

HCID 113914604-(6-Chloro-2-oxo-2H-1-benzopyran-4-yl)-butyramide수율 93%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

4-(6-Chloro-2-oxo-2H-1-benzopyran-4-yl)-butyronitrile (100 mg, 0.4 mmol) is dissolved in conc. H2SO4 (2 mL) and is stirred for 4 hrs. Ice and then H2O (20 mL) is added to the reaction mixture, and the resulting precipitate is filtered and is washed with H2O and Et2O. The solid is dried in vacuo to give the title compound (100 mg, 93%) as a white solid. 1H NMR (DMSO-d6, 400 MHz) δ 7.98 (1H, d, J=2 Hz), 7.68 (1H, dd, J=2, 9 Hz), 7.47 (1H, d, J=9 Hz), 7.32 (1H, broad s), 6.83 (1H, broad s), 6.43 (1H, s), 2.79 (2H, t, J=7 Hz), 2.20 (2H, t, J=7 Hz), 1.82 (2H, q, J=7 Hz); LCMS (MeCN—H2O, Luna 3μ C18(2) 30×4.6 mm) m/z (ES, Pos) calc. for C13H12ClNO3 m/z [M+H]=266, found 266.

후처리

  1. filtrationthe resulting precipitate is filtered
  2. washis washed with H2O and Et2O
  3. customThe solid is dried in vacuo

출처 및 근거

ORD 기록
ord-538f78f6e29e4d229a3d24555f34b414
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07538233B2

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