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Dichloromethane → 4-Benzylamino-6-methoxy-[1,5]naphthyridin-3-ol

HRID 1422923
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HRID 1422923 반응식
[CH2:1]([NH:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([O:19][CH3:20])[N:17]=2)[N:12]=[CH:11][C:10]=1Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(C1C=C(C(C)C)C(C2C(C)=C(C)C(C)=C(C)C=2P(C)C)=C(C)C=1)(C)C.[OH-:48].[K+].ClCCl>O1CCOCC1.O.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].CO>[CH2:1]([NH:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([O:19][CH3:20])[N:17]=2)[N:12]=[CH:11][C:10]=1[OH:48])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

9

반응물 4

HCID 6344DichloromethaneHCID 14797Potassium HydroxideHCID 67255893Benzyl-(3-bromo-6-methoxy-[1,5]naphthyridin-4-yl)-amineHCID 86671532(4',6'-Diisopropyl-3,4,5,6,2'-pentamethyl-biphenyl-2-yl)-dimethyl-phosphane

생성물 1

HCID 1363447114-Benzylamino-6-methoxy-[1,5]naphthyridin-3-ol수율 36.8%

시약·촉매·용매 4

HCID 9811564
Bis(dibenzylideneacetone)palladium
촉매
HCID 887Methanol용매
HCID 962Water용매2회
HCID 312751,4-Dioxane용매

실험 절차

Tris(dibenzylideneacetone)dipalladium(0) (10 mg, 0.011 mmol, 0.04 eq) is added at room temperature to a stirred solution of benzyl-(3-bromo-6-methoxy-[1,5]naphthyridin-4-yl)-amine (100 mg, 0.29 mmol, 1.0 eq) in dioxane (6 mL) and water (3 mL), followed by (4′,6′-diisopropyl-3,4,5,6,2′-pentamethyl-biphenyl-2-yl)-dimethyl-phosphane (8 mg, 0.016 mmol, 0.06 eq). After 10 minutes stirring at room temperature, a solution of potassium hydroxide (82 mg, 1.46 mmol, 5.0 eq) in water (3 mL) is added and the resulting mixture is stirred at 105° C. for 16 hours. The reaction mixture is cooled down to room temperature, extracted with ethyl acetate (3×10 mL) and water (10 mL) and the pH is adjusted to 6 by the addition of a 1N hydrochloric acid aqueous solution. The combined organic layers are dried over sodium sulfate, filtered and concentrated to give the crude product that is purified by column chromatography (silica gel, eluent: dichloromethane:methanol, 5:1, v/v) to afford 4-benzylamino-6-methoxy-[1,5]naphthyridin-3-ol as a light yellow solid (30 mg, 36% yield).

후처리

  1. stirringthe resulting mixture is stirred at 105° C. for 16 hours
  2. temperatureThe reaction mixture is cooled down to room temperature
  3. extractionextracted with ethyl acetate (3×10 mL) and water (10 mL)
  4. additionthe pH is adjusted to 6 by the addition of a 1N hydrochloric acid aqueous solution
  5. dry with materialThe combined organic layers are dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto give the crude product that
  9. customis purified by column chromatography (silica gel, eluent

출처 및 근거

ORD 기록
ord-745fbc17ed0a49a8917ca69a0bc361d7
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927541B2

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