Water → HCID 59514494, compound

HRID 2422140Notes

Reaction equation

HRID 2422140 reaction equation
[CH3:1][O:2][C:3](=[O:23])[CH2:4][C:5]1[C:6]([Cl:22])=[N:7][C:8]([CH2:14][C:15]2[CH:20]=[CH:19][C:18]([NH2:21])=[CH:17][CH:16]=2)=[N:9][C:10]=1[N:11]([CH3:13])[CH3:12].C1CN([P+](ON2N=NC3C=CC=CC2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.[CH:57]1[C:66]2[C:61](=[CH:62][CH:63]=[CH:64][CH:65]=2)[CH:60]=[CH:59][C:58]=1[C:67](O)=[O:68].O>CN(C=O)C>[Cl:22][C:6]1[C:5]([CH2:4][C:3]([O:2][CH3:1])=[O:23])=[C:10]([N:11]([CH3:12])[CH3:13])[N:9]=[C:8]([CH2:14][C:15]2[CH:16]=[CH:17][C:18]([NH:21][C:67]([C:58]3[CH:59]=[CH:60][C:61]4[C:66](=[CH:65][CH:64]=[CH:63][CH:62]=4)[CH:57]=3)=[O:68])=[CH:19][CH:20]=2)[N:7]=1

Participants

6

Reactant 4

HCID 962WaterHCID 71232-Naphthoic acidHCID 2724699PyBOPHCID 59514486Methyl 2-[(4-aminophenyl)methyl]-4-chloro-6-(dimethylamino)-5-pyrimidineacetate

Product 1

HCID 59514494HCID 59514494, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

To a mixture of methyl[2-(4-aminobenzyl)-4-chloro-6-(dimethylamino)pyrimidin-5-yl]acetate (0.090 g, 0.30 mmol) and PyBOP (0.187 g, 0.36 mmol) in anhydrous DMF (1 mL) at room temperature was added 2-naphthoic acid (0.062 g, 0.36 mmol). The resulting reaction mixture was stirred at room temperature for 3 hours at which time water was added and the resulting aqueous phase was extracted with EtOAc. The combined organic extracts was sequentially washed with 0.5N HCl, saturated NaHCO3, and brine, dried over anhydrous MgSO4, filtered, and concentrated in vacuo to give methyl {4-chloro-6-(dimethylamino)-2-[4-(2-naphthoylamino)benzyl]pyrimidin-5-yl}acetate as a colorless oil.

Workup

  1. customThe resulting reaction mixture
  2. additionwas added
  3. extractionthe resulting aqueous phase was extracted with EtOAc
  4. washThe combined organic extracts was sequentially washed with 0.5N HCl, saturated NaHCO3, and brine
  5. dry with materialdried over anhydrous MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-3f3670f928fe41aca1446e64d472cbb3
Source dataset
uspto-grants-2011_06
Patent number
US07960393B2

Reaction notes

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