Pyridine → HCID 22725169, compound

HRID 1066969Notes

Reaction equation

HRID 1066969 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:10]2[NH:15][C:14]([O:16][CH3:17])=[N:13][C:12]([CH3:18])=[C:11]2[C:19](=[O:21])[CH3:20])[CH:5]=[C:6]([F:9])[C:7]=1[F:8].N1C=CC=CC=1.Cl[C:29]([O:31][C:32]1[CH:37]=[CH:36][C:35]([N+:38]([O-:40])=[O:39])=[CH:34][CH:33]=1)=[O:30]>C(Cl)Cl>[F:1][C:2]1[CH:3]=[C:4]([CH:10]2[N:15]([C:29]([O:31][C:32]3[CH:33]=[CH:34][C:35]([N+:38]([O-:40])=[O:39])=[CH:36][CH:37]=3)=[O:30])[C:14]([O:16][CH3:17])=[N:13][C:12]([CH3:18])=[C:11]2[C:19](=[O:21])[CH3:20])[CH:5]=[C:6]([F:9])[C:7]=1[F:8]

Participants

5

Reactant 3

HCID 1049PyridineHCID 821294-Nitrophenyl chloroformateHCID 178494173HCID 178494173, compound

Product 1

HCID 22725169HCID 22725169, compoundYield 92%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 6-(3,4,5-trifluorophenyl)-1,6-dihydro-2-methoxy-5-acetyl-4-methylpyrimidine (2.8 g, 9.38 mmol) and pyridine (10 mL) in CH2Cl2 (200 mL) at 0-5° C., 4-nitrophenyl chloroformate (1.886 g, 9.38 mmol) was added and the mixture was allowed to warm to room temperature. After 12 hours solvent was evaporated and the residue was purified by flash column chromatography (SiO2, dichloromethane/EtOAc, 10%-15%) to obtain the product as a white powder (4.0 g, 92%).

Workup

  1. customAfter 12 hours solvent was evaporated
  2. customthe residue was purified by flash column chromatography (SiO2, dichloromethane/EtOAc, 10%-15%)

Sources & evidence

ORD record
ord-c8c70f322c254ce3adff3b20b4b3ddcb
Source dataset
uspto-grants-2001_06
Patent number
US06245773B1

Reaction notes

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