Sodium Hydroxide → Gsk-269984A

HRID 2356606Notes

Reaction equation

HRID 2356606 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][C:23]=2[F:29])=[C:6]([CH2:8][C:9]2[N:14]=[C:13]([C:15]([O:17]CC)=[O:16])[CH:12]=[CH:11][CH:10]=2)[CH:7]=1.[OH-].[Na+:31]>C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][C:23]=2[F:29])=[C:6]([CH2:8][C:9]2[N:14]=[C:13]([C:15]([O-:17])=[O:16])[CH:12]=[CH:11][CH:10]=2)[CH:7]=1.[Na+:31]

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 59384237Ethyl 6-(5-chloro-2-((4-chloro-2-fluorobenzyl)oxy)benzyl)picolinate

Product 1

HCID 23696973Gsk-269984A

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Ethyl 6-[(5-chloro-2-{[(4-chloro-2-fluorophenyl)methyl]oxy}phenyl)methyl]-2-pyridinecarboxylate (421.4 mg, 0.97 mmol) was suspended in ethanol (4 ml) and 2M sodium hydroxide (1 ml) and heated at 90° C. for 1.75 hours. Reaction complete after about 1 hour.

Workup

  1. customReaction complete after about 1 hour

Sources & evidence

ORD record
ord-70537d48873e4cba901481c0d29c3061
Source dataset
uspto-grants-2010_07
Patent number
US07759369B2

Reaction notes

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