benzyl (1-(5-(4-((1R,2S)-1-((bis(benzyloxy)-phosphoryl)oxy)-2-(2,2-difluoroacetamido)-3-fluoropropyl)phenyl)pyridin-2-yl)ethyl)carbamate → (1R,2S)-1-(4-(6-(1-aminoethyl)pyridin-3-yl)phenyl)-2-(2,2-difluoroacetamido)-3-fluoropropyl dihydrogen phosphate

HRID 1520550ノート

反応式

HRID 1520550 の反応式
C([O:8][P:9]([O:19][C@H:20]([C:30]1[CH:35]=[CH:34][C:33]([C:36]2[CH:37]=[CH:38][C:39]([CH:42]([NH:44]C(=O)OCC3C=CC=CC=3)[CH3:43])=[N:40][CH:41]=2)=[CH:32][CH:31]=1)[C@H:21]([NH:24][C:25](=[O:29])[CH:26]([F:28])[F:27])[CH2:22][F:23])([O:11]CC1C=CC=CC=1)=[O:10])C1C=CC=CC=1>[Pd].C(O)C.O>[P:9]([OH:11])([OH:10])([O:19][C@H:20]([C:30]1[CH:31]=[CH:32][C:33]([C:36]2[CH:41]=[N:40][C:39]([CH:42]([NH2:44])[CH3:43])=[CH:38][CH:37]=2)=[CH:34][CH:35]=1)[C@H:21]([NH:24][C:25](=[O:29])[CH:26]([F:28])[F:27])[CH2:22][F:23])=[O:8]

参加物

5

実験手順

Palladium on carbon (1:9, 23 mg, 0.022 mmol) is added to the product of step 4, Example 95A (235 mg, 0.308 mmol) in ethanol (5 mL) and water (1 mL). The mixture is evacuated with nitrogen three times and stirred under hydrogen for 5 hours. The reaction mixture is filtered through a 4 mL pad of solka flok and rinsed with alternating 4 mL rinses of ethanol and water ten times. The solvent is removed under reduced pressure to give the crude product, which is taken up in water (5 mL) and filtered through a 0.45 um filter disk, rinsing with water (2 mL). The filtrate is freeze dried to give the title product (126 mg): 1H NMR δ 8.75 (1H, s), 8.07 (1H, d), 7.63 (2H, d), 7.52-7.48 (4H, m), 6.00 (1H, t), 5.42 (1H, d), 4.82 (1H, dd), 4.64-4.43 (4H, m), 1.62 (3H, d); m/z: 447.12.

後処理

  1. customThe mixture is evacuated with nitrogen three times
  2. filtrationThe reaction mixture is filtered through a 4 mL pad of solka flok
  3. washrinsed
  4. customThe solvent is removed under reduced pressure
  5. customto give the crude product, which
  6. filtrationfiltered through a 0.45 um
  7. filtrationfilter disk
  8. washrinsing with water (2 mL)
  9. customdried

出典と根拠

ORDレコード
ord-3d29ccac32274f59adceb3472950553d
出典データセット
uspto-grants-2015_07
特許番号
US09073894B2

反応ノート

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