Imidazole → HCID 22176416、化合物

HRID 1797261

反応式

HRID 1797261 の反応式
N[CH:2]([CH2:5][O:6][C:7]([CH3:10])([CH3:9])C)[CH2:3]O.C(O[BH-](O[C:21](=[O:23])[CH3:22])OC(=O)C)(=O)C.[Na+].II.[NH:27]1C=CN=C1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[F:51][C:52]1C=CC(OC2CCNCC2)=[CH:54][CH:53]=1.[CH:65]([N:68]([CH:71](C)C)[CH2:69]C)(C)C.[C:74]([C:76]1[CH:77]=[CH:78][C:79]([O:87][CH3:88])=[C:80](/[CH:82]=[CH:83]/[C:84]([OH:86])=O)[CH:81]=1)#[N:75].F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1>C(O)(=O)C.CN(C=O)C.CN(C=O)C>[C:74]([C:76]1[CH:77]=[CH:78][C:79]([O:87][CH3:88])=[C:80](/[CH:82]=[CH:83]/[C:84]([NH:27][CH:22]([CH2:21][OH:23])[CH2:71][N:68]2[CH2:65][CH2:9][CH:7]([O:6][C:5]3[CH:2]=[CH:3][C:52]([F:51])=[CH:53][CH:54]=3)[CH2:10][CH2:69]2)=[O:86])[CH:81]=1)#[N:75]

参加物

12

反応条件

温度
20 °C

実験手順

To a suspension of 2-(formyl-3-methoxyphenoxy)ethyl polystyrene (AMEBA) resin (ex Novabiochem) (2.13 g, 3.40 mmol) in a mixture of acetic acid/DMF (60 ml, 1:100 v/v) is added 2-amino-3-tert-butoxy-propan-1-ol and sodium triacetoxyborohydride (1.44 g, 6.80 mmol) and the mixture is shaken for 18 hours at 20° C., then filtered. The resin obtained is washed with methanol, DMF and dichloromethane (DCM), then dried under vacuum. A THF/acetonitrile mixture (20 ml, 1:1 v/v) is added to the dried resin followed by iodine (4.30 g, 18.85 mmol), imidazole (1.16 g, 17.00 mmol) and triphenylphosphine (4.46 g, 17.00 mmol). The suspension obtained is shaken for 6 hours at 20° C., then filtered. The resin is washed with THF and dried under vacuum. To the freshly prepared resin obtained (0.30 g, 0.48 mmol) is added a solution of 4-(4-fluoro-phenoxy)-piperidine (309 mg, 1.00 mmol) dissolved in DMF (2 ml) and diisopropylethylamine (62.4 mg, 0.48 mmol). The mixture is heated at 55° C. for 8 hours. The resulting mixture is filtered and the resin is washed with DMF. To the washed resin are added (E)-3-(5-cyano-2-methoxy-phenyl)-acrylic acid (0.27 g, 1.05 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluroniumhexafluoro-phosphate (547 mg, 1.44 mmol) diisopropylethylamine (186 mg, 1.44 mmol) and DMF (4 ml) and the mixture is shaken at 20° C. for 18 hours, then washed with DMF and methanol, after which it is treated with trifluoroacetic acid/DCM (6 ml, 1:1 v/v) at 20° C. for 1 hour to remove the product from the resin. The resulting mixture is filtered and the filtrate evaporated under vacuum to give the product, [MH]+ 453.9.

後処理

  1. filtrationfiltered
  2. customThe resin obtained
  3. washis washed with methanol, DMF and dichloromethane (DCM)
  4. customdried under vacuum
  5. additionA THF/acetonitrile mixture (20 ml, 1:1 v/v) is added to the dried resin
  6. customThe suspension obtained
  7. stirringis shaken for 6 hours at 20° C.
  8. filtrationfiltered
  9. washThe resin is washed with THF
  10. customdried under vacuum
  11. customTo the freshly prepared resin obtained (0.30 g, 0.48 mmol)
  12. temperatureThe mixture is heated at 55° C. for 8 hours
  13. filtrationThe resulting mixture is filtered
  14. washthe resin is washed with DMF
  15. stirringthe mixture is shaken at 20° C. for 18 hours
  16. washwashed with DMF and methanol
  17. additionafter which it is treated with trifluoroacetic acid/DCM (6 ml, 1:1 v/v) at 20° C. for 1 hour
  18. customto remove the product from the resin
  19. filtrationThe resulting mixture is filtered
  20. customthe filtrate evaporated under vacuum
  21. customto give the product, [MH]+ 453.9

出典と根拠

ORDレコード
ord-792f3ba8595d4991a482372e7d1739a4
出典データセット
uspto-grants-2006_04
特許番号
US07034042B2

関連ノート

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