Hydrochloric Acid → HCID 67314715, 화합물

HRID 1011336노트

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HRID 1011336 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].[CH3:11][C:12]1[N:17]=[C:16]2[CH2:18][O:19][C:20](=O)[C:15]2=[CH:14][CH:13]=1.Cl>C1COCC1>[CH3:11][C:12]1[N:17]=[C:16]2[CH2:18][O:19][C:20](=[C:3]3[C:4]4[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=4)[NH:1][C:2]3=[O:10])[C:15]2=[CH:14][CH:13]=1

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 321710OxindoleHCID 58478770HCID 58478770, 화합물

생성물 1

HCID 67314715HCID 67314715, 화합물수율 30%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매3회

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온도
90 °C

실험 절차

A solution of 1,3-dihydro-indol-2-one (200 mg, 1.5 mmol.) in THF (2 mL) is placed under an argon atmosphere and cooled in an ice bath. A solution of Li bis(trimethylsilyl)amide (4.0 mL of a 1M solution in THF, 4.0 mmol) is added slowly at 0° C. and the resulting solution is stirred for 10 min. The ice-bath is then removed and a solution of 2-methyl-7H-furo[3,4-b]pyridin-5-one (150 mg, 1.00 mmol) in THF (6 mL) is added dropwise to the reaction mixture. The resulting solution is stirred for 4 h and then poured into 10% aqueous HCl solution (50 mL). After 10 min at room temperature, the reaction is heated to ˜90° C. for 45 min followed by stirring at room temperature for 36 h. The solid which precipitated from solution is collected by filtration and washed sequentially with small volumes of MeOH, EtOAc, Et2O and dried under vacuum to give the title compound as a yellow solid (78 mg, 30%).

후처리

  1. temperaturecooled in an ice bath
  2. customThe ice-bath is then removed
  3. stirringThe resulting solution is stirred for 4 h
  4. waitAfter 10 min at room temperature
  5. stirringby stirring at room temperature for 36 h
  6. customThe solid which precipitated from solution
  7. filtrationis collected by filtration
  8. washwashed sequentially with small volumes of MeOH, EtOAc, Et2O
  9. customdried under vacuum

출처 및 근거

ORD 기록
ord-fce2c34f76a241128ccf0f75991075a0
출처 데이터셋
uspto-grants-2011_07
특허 번호
US07977351B2

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