Sodium hydride → 4-Chloro-6-methyl-11h-5-oxa-10-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl ester

HRID 2425086노트

반응식

HRID 2425086 반응식
[H-].[Na+].[CH3:3][O:4][C:5](=[O:24])[C:6]1[CH:11]=[C:10]([CH3:12])[C:9](Br)=[C:8]([S:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([Cl:22])[C:17]=2[OH:23])[CH:7]=1>CN(C=O)C>[CH3:3][O:4][C:5]([C:6]1[CH:11]=[C:10]([CH3:12])[C:9]2[O:23][C:17]3[C:18]([Cl:22])=[CH:19][CH:20]=[CH:21][C:16]=3[CH2:15][S:14][C:8]=2[CH:7]=1)=[O:24]

참가 물질

4

반응물 2

HCID 24758Sodium hydrideHCID 67246085HCID 67246085, 화합물

생성물 1

HCID 672474734-Chloro-6-methyl-11h-5-oxa-10-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl ester

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

Sodium hydride (1.65 g, 0.068 mol) was added portionwise to a solution of compound of Example 15a (23 g, 0.057 mol) in DMF (600 mL) and stirred at 80° C. for 10 h. The solvent was removed, and chloroform (300 mL) was added. The organic layer was washed with 10% HCl (2×80 mL), followed by water (100 mL), and brine and dried over anhydrous sodium sulphate. The solvent was removed and the crude product obtained was purified by column chromatography (silica gel, ethyl acetate/pet ether) to obtain the title compound. Yield: 9 g, (49%); 1H NMR (CDCl3, 300 MHz): δ 2.50 (s, 3H, CH3), 3.91 (s, 3H, OCH3), 4.21 (s, 2H, CH2), 7.05 (m, 2H, Ar), 7.28 (d, 1H, Ar), 7.60 (d, 2H, Ar); MS: m/e (EI) 320 (M+).

후처리

  1. customThe solvent was removed
  2. additionchloroform (300 mL) was added
  3. washThe organic layer was washed with 10% HCl (2×80 mL)
  4. dry with materialdried over anhydrous sodium sulphate
  5. customThe solvent was removed
  6. customthe crude product obtained
  7. customwas purified by column chromatography (silica gel, ethyl acetate/pet ether)

출처 및 근거

ORD 기록
ord-0024f9a9ce30498eb36d14b2b9b94075
출처 데이터셋
uspto-grants-2011_06
특허 번호
US07964631B2

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