Water → HCID 66960350, compound

HRID 1446594Notes

Reaction equation

HRID 1446594 reaction equation
[H-].[Na+].[N:3]1([C:9]2[CH:18]=[C:17]3[C:12]([CH2:13][CH2:14][CH2:15][CH:16]3[NH:19][C:20](=[O:41])/[C:21](=[CH:26]/[C:27]3[CH:32]=[CH:31][C:30]([N:33]4[CH:37]=[C:36]([CH3:38])[N:35]=[CH:34]4)=[C:29]([O:39][CH3:40])[CH:28]=3)/[CH2:22][CH2:23][CH2:24]Cl)=[CH:11][CH:10]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.O.C(OCC)(=O)C>CN(C=O)C>[CH3:40][O:39][C:29]1[CH:28]=[C:27]([CH:32]=[CH:31][C:30]=1[N:33]1[CH:37]=[C:36]([CH3:38])[N:35]=[CH:34]1)/[CH:26]=[C:21]1/[C:20](=[O:41])[N:19]([CH:16]2[C:17]3[C:12](=[CH:11][CH:10]=[C:9]([N:3]4[CH2:8][CH2:7][O:6][CH2:5][CH2:4]4)[CH:18]=3)[CH2:13][CH2:14][CH2:15]2)[CH2:24][CH2:23][CH2:22]/1

Participants

6

Procedure

Sodium hydride (containing mineral oil at 40%, 37.8 mg) was added to a solution of (E)-5-chloro-2-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)-benzylidene)valeric acid (7-morpholin-4-yl-1,2,3,4-tetrahydronaphthalen-1-yl)amide (213 mg) in DMF (5.0 mL) at 0° C., and the reaction solution was stirred for 30 minutes. After confirming that the raw materials disappeared, water and ethyl acetate were added to the reaction solution and the organic layer was partitioned. The organic layer was washed with brine, and then dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (elution solvent:heptane-ethyl acetate system→ethyl acetate-methanol system) to obtain 195 mg of (E)-3-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene)-1-(7-morpholin-4-yl-1,2,3,4-tetrahydronaphthalen-1-yl)piperidin-2-one as a racemate.

Workup

  1. customthe organic layer was partitioned
  2. washThe organic layer was washed with brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by silica gel chromatography (elution solvent:heptane-ethyl acetate system→ethyl acetate-methanol system)

Sources & evidence

ORD record
ord-de5ff20061d546b995e1425b53526d0a
Source dataset
uspto-grants-2010_02
Patent number
US07667041B2

Reaction notes

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