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Dimethylformamide → HCID 135855967, 화합물

HRID 983444
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HRID 983444 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].CN(C=O)C.[H-].[Na+].Cl[C:19]1[N:24]=[CH:23][N:22]=[C:21]([NH:25][C:26]2[CH:31]=[C:30]([O:32][CH3:33])[C:29]([O:34][CH3:35])=[C:28]([O:36][CH3:37])[CH:27]=2)[N:20]=1>C1COCC1>[CH3:33][O:32][C:30]1[CH:31]=[C:26]([NH:25][C:21]2[N:20]=[CH:19][N:24]=[C:23]([C:3]3[C:4]4[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=4)[NH:1][C:2]=3[OH:10])[N:22]=2)[CH:27]=[C:28]([O:36][CH3:37])[C:29]=1[O:34][CH3:35]
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참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 24758Sodium hydrideHCID 321710OxindoleHCID 22028121HCID 22028121, 화합물

생성물 1

HCID 135855967HCID 135855967, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Oxindole (176 mg, 1.32 mmol) was dissolved in a 1:1 mixture of THF:DMF (4 mL), under N2, at RT. NaH (53 mg of a 60% suspension in mineral oil, 1.32 mmol) was added, which produced a vigorous gas evolution. This mixture was stirred for 30 min at RT, then (4-chloro-[1,3,5]triazin-2-yl)-(3,4,5-trimethoxy-phenyl)amine (156 mg, 0.53 mmol) was added and the reaction was heated to 80° C. for 2 h. The reaction was cooled to RT, partially concentrated under reduced pressure, diluted with EtOAc, then extracted with water. The water extract was back extracted two times with fresh EtOAc. All of the EtOAc extracts were washed with brine, combined, dried over NaSO4, filtered and concentrated. The recovered material was purified by preparative HPLC (5 to 100% CH3CN:H2O (0.1% TFA buffer) over 10 min at 20 mL/min) Crystals formed in the recovered eluant, which were recovered by vacuum filtration, washed with water, and dried under high vacuum giving 3-[4-(3,4,5-trimethoxy-phenylamino)-[1,3,5]triazin-2-yl]-1H-indol-2-ol as a yellow solid: MS m/z=394 [M+H]+. Calc'd for C20H19N5O4: 393.14.

후처리

  1. customat RT
  2. customwhich produced a vigorous gas evolution
  3. temperaturethe reaction was heated to 80° C. for 2 h
  4. temperatureThe reaction was cooled to RT
  5. concentrationpartially concentrated under reduced pressure
  6. additiondiluted with EtOAc
  7. extractionextracted with water
  8. extractionThe water extract
  9. extractionwas back extracted two times with fresh EtOAc
  10. washAll of the EtOAc extracts were washed with brine
  11. dry with materialdried over NaSO4
  12. filtrationfiltered
  13. concentrationconcentrated
  14. customThe recovered material was purified by preparative HPLC (5 to 100% CH3CN:H2O (0.1% TFA buffer) over 10 min at 20 mL/min) Crystals
  15. customformed in the recovered eluant, which
  16. filtrationwere recovered by vacuum filtration
  17. washwashed with water
  18. customdried under high vacuum

출처 및 근거

ORD 기록
ord-c8a0b608e22e4c25aecf21b5a2ed08a5
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06864255B2

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