Sodium Hydroxide → HCID 66955807, compound

HRID 1399645Notes

Reaction equation

HRID 1399645 reaction equation
[CH3:1][C:2]1[C:7]([CH:8]([CH2:13][CH2:14][CH3:15])[C:9]([O:11]C)=[O:10])=[C:6]([O:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[N:5]=[C:4]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[N:3]=1.[OH-].[Na+]>CO>[CH3:1][C:2]1[C:7]([CH:8]([CH2:13][CH2:14][CH3:15])[C:9]([OH:11])=[O:10])=[C:6]([O:16][C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[N:5]=[C:4]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[N:3]=1

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 66955927Methyl 2-(4-methyl-6-phenoxy-2-phenylpyrimidin-5-yl)pentanoate

Product 1

HCID 66955807HCID 66955807, compoundYield 70.9%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

This compound was prepared according to general method D from methyl 2-(4-methyl-6-phenoxy-2-phenylpyrimidin-5-yl)pentanoate (0.082 g; 0.218 mmol), sodium hydroxide 10N (0.218 mL; 2.18 mmol) in methanol (2 mL) to afford 0.056 g (68%) of the title compound as a white solid.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-270657ae8f6c4fdaa45d5d9c79b8f9b0
Source dataset
uspto-grants-2014_12
Patent number
US08906906B2

Reaction notes

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