Hydrochloric Acid → 9-Chloromethyl-7-oxo-2,3,6,7-tetrahydro[1,4]dioxino[2,3-g]quinoline-8-carboxylic acid ethyl ester

HRID 411847

반응식

HRID 411847 반응식
[NH2:1][C:2]1[C:3]([C:12](=O)[CH2:13][Cl:14])=[CH:4][C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[CH:11]=1.C(N([CH2:21][CH3:22])CC)C.C([CH:25]([C:29](Cl)=[O:30])[C:26](Cl)=[O:27])C.Cl.[OH2:33]>C(#N)C>[CH2:21]([O:33][C:29]([C:25]1[C:26](=[O:27])[NH:1][C:2]2[CH:11]=[C:6]3[O:7][CH2:8][CH2:9][O:10][C:5]3=[CH:4][C:3]=2[C:12]=1[CH2:13][Cl:14])=[O:30])[CH3:22]

참가 물질

7

실험 절차

To a mixture of 1-(7-amino-2,3-dihydro-benzo[1,4]dioxin-6-yl)-2-chloro-ethanone (230 g. 1.01 mol) prepared as described in Intermediate 12, in acetonitrile (1.5 L) and triethylamine (197 mL, 1.41 mol, 1.4 eq) is added ethyl malonyl chloride (180 mL, 1.41 mol, 1.4 eq) over 0.5 h while keeping the reaction temperature less than 30° C. with an ice bath. After the addition is complete the reaction is stirred 1.5 h at room temperature. A second charge of Triethylamine (140 mL, 1.01 mol, 1.0 eq) is added and the reaction is stirred for 4.5 hours. Water (2.1 L) is added slowly followed by conc. HCl (115 mL). The slurry is stirred overnight at rt, filtered, and the solid washed with water (460 mL). The solid is then dried under high vacuum (about 1 mm Hg) at 40° C. to give 270 g (83%) 9-chloromethyl-7-oxo-2,3,6,7-tetrahydro[1,4]dioxino[2,3-g]quinoline-8-carboxylic acid ethyl ester as a yellow solid. HRMS (EI+): calc for C15H14NO5Cl: 323.0561, Found: 323.0556.

후처리

  1. customprepared
  2. customthe reaction temperature less than 30° C.
  3. additionAfter the addition
  4. additionis added
  5. stirringthe reaction is stirred for 4.5 hours
  6. stirringThe slurry is stirred overnight at rt
  7. filtrationfiltered
  8. washthe solid washed with water (460 mL)
  9. customThe solid is then dried under high vacuum (about 1 mm Hg) at 40° C.

출처 및 근거

ORD 기록
ord-fd46dc862bf9473d8dd7dade3870ea4e
출처 데이터셋
uspto-grants-2003_05
특허 번호
US06559309B2

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