Methanol → 2,2-Dichloro-N-{(1S,2R)-2-[4-(6-dimethylamino-methyl-pyridin-3-yl)-phenyl]-1-fluoromethyl-2-hydroxy-ethyl}-acetamide

HRID 525591

Reaction equation

HRID 525591 reaction equation
[NH2:1][C@H:2]([CH2:21][F:22])[C@H:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:12]=[N:13][C:14](CN(C)C)=[CH:15][CH:16]=2)=[CH:7][CH:6]=1)[OH:4].[Cl:23][CH:24]([Cl:30])[C:25](OCC)=[O:26].[CH2:31]([N:33](CC)[CH2:34]C)C.[CH3:38]O>>[Cl:23][CH:24]([Cl:30])[C:25]([NH:1][C@H:2]([CH2:21][F:22])[C@@H:3]([C:5]1[CH:6]=[CH:7][C:8]([C:11]2[C:12]([CH3:38])=[N:13][C:14]([N:33]([CH3:34])[CH3:31])=[CH:15][CH:16]=2)=[CH:9][CH:10]=1)[OH:4])=[O:26]

Participants

5

Procedure

To a stirred solution of (1S,2S)-2-Amino-1-[4-(6-dimethylaminomethyl-pyridin-3-yl)-phenyl]-3-fluoro-propan-1-ol (60 mg, 0.143 mmol) in dry methanol (0.26 mL) is added ethyl dichloroacetate (45 mg, 0.287 mmol) and triethylamine (29 mg, 0.287 mmol) at room temperature and reaction mixture stirred for 24 hours. Solvent is evaporated in vacuo and the crude material purified by column chromatography eluting in 6% methanol in CH2Cl2 to afford title compound (13 mg): 1H-NMR (400 MHz, DMSO-d6) δ: 2.20 (s, 6H), 3.54 (s, 2H), 4.17-4.24 (m, 1H), 4.27-4.31 (m, 0.5H), 4.39-4.41 (m, 0.5H), 4.56-4.58 (m, 0.5H), 4.59-4.71 (m, 0.5H), 4.89 (m, 1H), 4.99 (d, 1H, J=4 Hz), 6.52 (s, 1H), 7.45-7.49 (m, 3H), 7.68 (d, 2H, J=8.24 Hz), 8.03 (dd, 1H, J1=8.08 Hz, J2=2.4 Hz), 8.64 (d, 1H, J=8.8 Hz), 8.77 (d, 1H, J=2.04 Hz). LC-MS (m/z): [M+H]=414.

Workup

  1. customreaction mixture
  2. customSolvent is evaporated in vacuo
  3. customthe crude material purified by column chromatography
  4. washeluting in 6% methanol in CH2Cl2

Sources & evidence

ORD record
ord-db582ffe85bb4ce2a13313fe90691869
Source dataset
uspto-grants-2016_05
Patent number
US09340564B2

Linked notes

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