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Ammonium Chloride → HCID 117987829, compound

HRID 2206063
Notes
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Reaction equation

HRID 2206063 reaction equation
CCN(C(C)C)C(C)C.CCCCCC.C([Li])CCC.[Br:21][C:22]1[CH:23]=[C:24]([F:30])[C:25]([O:28][CH3:29])=[N:26][CH:27]=1.[CH:31]1([CH:36]=[O:37])[CH2:35][CH2:34][CH2:33][CH2:32]1.[Cl-].[NH4+]>C1COCC1>[Br:21][C:22]1[C:23]([CH:36]([CH:31]2[CH2:35][CH2:34][CH2:33][CH2:32]2)[OH:37])=[C:24]([F:30])[C:25]([O:28][CH3:29])=[N:26][CH:27]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 25517Ammonium ChlorideHCID 70106CyclopentanecarbaldehydeHCID 81531DiisopropylethylamineHCID 148370115-Bromo-3-fluoro-2-methoxypyridineHCID 178418244HCID 178418244, compound

Product 1

HCID 117987829HCID 117987829, compoundYield 29.1%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-78 °C

Procedure

To a solution of DIEA (0.827 mL) in THF (90 mL) was added 1.6 M n-butyllithium hexane solution (3.64 mL) at −78° C., and the mixture was stirred under argon atmosphere at −78° C. for 30 min. To the reaction mixture was added a solution of 5-bromo-3-fluoro-2-methoxypyridine (1.00 g) in THF (30 mL) at −78° C., and the mixture was stirred under argon atmosphere at −78° C. for 1 hr. To the reaction mixture was added cyclopentanecarbaldehyde (0.572 g) at −78° C., and the mixture was stirred under argon atmosphere at −78° C. for 1 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution at −78° C., and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (430 mg).

Workup

  1. stirringthe mixture was stirred under argon atmosphere at −78° C. for 1 hr
  2. stirringthe mixture was stirred under argon atmosphere at −78° C. for 1 hr
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe organic layer was washed with saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

Sources & evidence

ORD record
ord-ec32e8677ef1416bb497deb3cd0f61a1
Source dataset
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09371320B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes