Hydrochloric Acid → 4'-[[[2-[4-Fluorophenoxy]-pyridine-3-carbonyl]-amino]-methyl]-biphenyl-3-carboxylic acid

HRID 480086Notes

Reaction equation

HRID 480086 reaction equation
C[O:2][C:3]([C:5]1[CH:6]=[C:7]([C:11]2[CH:16]=[CH:15][C:14]([CH2:17][NH:18][C:19]([C:21]3[C:22]([O:27][C:28]4[CH:33]=[CH:32][C:31]([F:34])=[CH:30][CH:29]=4)=[N:23][CH:24]=[CH:25][CH:26]=3)=[O:20])=[CH:13][CH:12]=2)[CH:8]=[CH:9][CH:10]=1)=[O:4].[OH-].[Na+].Cl.CO.ClCCl>C(O)(C)(C)C.O>[F:34][C:31]1[CH:32]=[CH:33][C:28]([O:27][C:22]2[C:21]([C:19]([NH:18][CH2:17][C:14]3[CH:15]=[CH:16][C:11]([C:7]4[CH:8]=[CH:9][CH:10]=[C:5]([C:3]([OH:4])=[O:2])[CH:6]=4)=[CH:12][CH:13]=3)=[O:20])=[CH:26][CH:25]=[CH:24][N:23]=2)=[CH:29][CH:30]=1

Participants

7

Procedure

A mixture of 300 mg (0.66 mmol.) 4′-[[[2-[4-Fluorophenoxy]-pyridine-3-carbonyl]-amino]-methyl]-biphenyl-3-carboxylic acid methyl ester and 1.6 mL 1.0 N NaOH in 10 mL t-butanol and 3 mL water and refluxed for 4 hours. The mixture was poured into water, acidified to pH 1 with 2N HCl, then extracted with ethyl acetate. The ethyl acetate extracted were combined, washed successively with water, brine then dried (MgSO4) and concentrated to give an oil. Chromatography on Silica Gel eluting with methanol/dichloromethane (1:40) yielded a foam. Recrystallization from ethyl acetate/hexanes afforded 151 mg 4′-[[[2-[4-Fluorophenoxy]-pyridine-3-carbonyl]-amino]-methyl]-biphenyl-3-carboxylic acid as a solid, mp 184-6° C.

Workup

  1. temperaturerefluxed for 4 hours
  2. extractionextracted with ethyl acetate
  3. extractionThe ethyl acetate extracted
  4. washwashed successively with water, brine
  5. dry with materialthen dried (MgSO4)
  6. concentrationconcentrated
  7. customto give an oil
  8. customRecrystallization from ethyl acetate/hexanes

Sources & evidence

ORD record
ord-4e1a4cf5a63240cba2b86fccef68b36d
Source dataset
uspto-grants-2003_11
Patent number
US06649633B2

Reaction notes

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