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Citric Acid → (+/-)-2-Methoxy-3-{[5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}propan-1-ol

HRID 1926914
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HRID 1926914 반응식
[CH3:1][O:2][CH:3]([CH2:6][OH:7])[CH2:4][OH:5].Cl[C:9]1[C:10]2[C:17]([C:18]3[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=3)=[C:16]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[O:15][C:11]=2[N:12]=[CH:13][N:14]=1.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>C1COCC1.C(OC)(C)(C)C.O>[CH3:1][O:2][CH:3]([CH2:6][O:7][C:9]1[C:10]2[C:17]([C:18]3[CH:19]=[CH:20][C:21]([O:24][CH3:25])=[CH:22][CH:23]=3)=[C:16]([C:26]3[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=3)[O:15][C:11]=2[N:12]=[CH:13][N:14]=1)[CH2:4][OH:5]
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참가 물질

7

반응물 3

HCID 311Citric AcidHCID 111709312-Methoxypropane-1,3-diolHCID 580168154-Chloro-5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidine

생성물 1

HCID 58016954(+/-)-2-Methoxy-3-{[5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]oxy}propan-1-ol

시약·촉매·용매 3

HCID 962Water용매
HCID 8028
Tetrahydrofuran
용매
2회
HCID 15413tert-Butyl methyl ether용매

실험 절차

Put 1.014 g (9.65 mmol) 2-methoxypropane-1,3-diol in 20 ml THF. Add 542 mg (4.825 mmol) potassium tert.-butylate and stir for 15 min at RT. Then cool to 0° C. and add a solution of 650 mg (1.93 mmol) 4-chloro-5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidine in 10 ml THF dropwise in the space of 30 min. Then leave to return to RT and stir overnight at RT. Next, dilute with tert.-butylmethyl ether and water. Acidify with 10% citric acid solution and separate the phases. Re-extract the aqueous phase once with tert.-butylmethyl ether. Combine the organic phases and wash once with satd. sodium chloride solution. Then dry over magnesium sulphate and concentrate by evaporation. Purify the residue by chromatography on silica gel (solvent: cyclohexane/ethyl acetate 7:3); 587 mg (74.8% of theor.) of the target compound is obtained.

후처리

  1. temperatureThen cool to 0° C.
  2. customThen leave
  3. customto return to RT
  4. stirringstir overnight at RT
  5. customseparate the phases
  6. washwash once with satd
  7. dry with materialThen dry over magnesium sulphate
  8. concentrationconcentrate by evaporation
  9. customPurify the residue by chromatography on silica gel (solvent: cyclohexane/ethyl acetate 7:3)
  10. custom587 mg (74.8% of theor.) of the target compound is obtained

출처 및 근거

ORD 기록
ord-c66f78d5d9bf4b85829f5b6b05c50ba6
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08183246B2

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