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Ethyl Acetate → HCID 178487875, compound

HRID 2273262
Notes
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Reaction equation

HRID 2273262 reaction equation
[C:1]([O:5][C:6](=[O:17])[NH:7][C@H:8]1[CH2:13][CH2:12][C@H:11]([CH2:14][CH:15]=[O:16])[CH2:10][CH2:9]1)([CH3:4])([CH3:3])[CH3:2].[Cl:18][C:19]1[CH:20]=[N:21][C:22]2[C:27]([C:28]=1[CH:29]=[O:30])=[N:26][C:25]([O:31][CH3:32])=[CH:24][CH:23]=2.N1CCC[C@H]1C(O)=O.C(OCC)(=O)C>CS(C)=O.O>[C:1]([O:5][C:6](=[O:17])[NH:7][C@H:8]1[CH2:9][CH2:10][C@H:11]([CH:14]([CH:15]=[O:16])[CH:29]([C:28]2[C:27]3[C:22](=[CH:23][CH:24]=[C:25]([O:31][CH3:32])[N:26]=3)[N:21]=[CH:20][C:19]=2[Cl:18])[OH:30])[CH2:12][CH2:13]1)([CH3:4])([CH3:2])[CH3:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 8857Ethyl AcetateHCID 145742L-ProlineHCID 866715503-Chloro-6-methoxy-[1,5]naphthyridine-4-carbaldehydeHCID 178453924HCID 178453924, compound

Product 1

HCID 178487875HCID 178487875, compoundYield 39%

Reagents, catalysts & solvents 2

HCID 679
Dimethyl Sulfoxide
Solvent
HCID 962WaterSolvent

Procedure

A solution of [trans-4-(2-oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (3.1 g, 25.1 mmol, 1.0 eq), 3-chloro-6-methoxy-[1,5]naphthyridine-4-carbaldehyde (5.6 g, 25.1 mmol, 1.0 eq) and L-proline (1.16 mg, 10.1 mmol, 0.4 eq) in dimethyl sulfoxide (100 mL) and water (15 mL) is stirred at room temperature for 16 hours. The reaction mixture is then extracted with ethyl acetate (500 mL) and water (500 mL). The organic layer is washed with brine (300 mL), dried over magnesium sulfate, filtered and concentrated to give a residue that is purified by column chromatography (silica gel, eluent: ethyl acetate:petroleum ether, 1:1, v/v) to afford {trans-4-[2-(3-chloro-6-methoxy-[1,5]naphthyridin-4-yl)-1-formyl-2-hydroxy-ethyl]-cyclohexyl}-carbamic acid tert-butyl ester as a light yellow solid (4.5 g, 39% yield).

Workup

  1. extractionThe reaction mixture is then extracted with ethyl acetate (500 mL) and water (500 mL)
  2. washThe organic layer is washed with brine (300 mL)
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customto give a residue that
  7. customis purified by column chromatography (silica gel, eluent

Sources & evidence

ORD record
ord-9fc56fc6f2e8450c94044cba211303ca
Source dataset
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09120822B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes