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Hydrochloric Acid → (S)-2-[4-(2-fluoro-5-methyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid

HRID 19092
Notes
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Reaction equation

HRID 19092 reaction equation
C[O:2][C:3](=[O:24])[C@@H:4]([N:9]1[CH2:13][C:12]([O:14][C:15]2[CH:20]=[C:19]([CH3:21])[CH:18]=[CH:17][C:16]=2[F:22])=[CH:11][C:10]1=[O:23])[CH2:5][CH:6]([CH3:8])[CH3:7].O.[OH-].[Li+].Cl>O1CCCC1.O>[F:22][C:16]1[CH:17]=[CH:18][C:19]([CH3:21])=[CH:20][C:15]=1[O:14][C:12]1[CH2:13][N:9]([C@@H:4]([CH2:5][CH:6]([CH3:8])[CH3:7])[C:3]([OH:24])=[O:2])[C:10](=[O:23])[CH:11]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 168937Lithium hydroxide, monohydrateHCID 66894723(S)-2-[4-(2-fluoro-5-methyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid methyl ester

Product 1

HCID 66894221(S)-2-[4-(2-fluoro-5-methyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acidYield 90%

Reagents, catalysts & solvents 2

HCID 962
Water
Solvent
2×
HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
25 °C

Procedure

A mixture of (S)-2-[4-(2-fluoro-5-methyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid methyl ester (0.59 g, 1.77 mmol) in tetrahydrofuran (13.3 mL) and water (4.4 mL) was treated with lithium hydroxide monohydrate (89 mg, 2.13 mmol). The reaction was stirred at 25° C. overnight. At this time, the reaction was diluted with water (75 mL), acidified with a 3N aqueous hydrochloric acid solution and then extracted with 10% methanol/dichloromethane (3×50 mL). The combined organics were dried over sodium sulfate, filtered and concentrated in vacuo to afford (S)-2-[4-(2-fluoro-5-methyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid (0.51 g, 90%) as an off-white solid: HR-ES-MS m/z calculated for C17H20NO4F [M+H]+ 322.1449, observed 322.1447; 1H NMR (300 MHz, DMSO-d6) δ ppm 0.84 (d, J=6.4 Hz, 3H), 0.90 (d, J=6.4 Hz, 3H), 1.44 (br. s., 1H), 1.51-1.66 (m, 1H), 1.66-1.84 (m, 1H), 2.29 (s, 3H), 4.13 (d, J=18.1 Hz, 1H), 4.25 (d, J=18.1 Hz, 1H), 4.60 (dd, J=11.3, 4.1 Hz, 1H), 4.86 (s, 1H), 7.09-7.19 (m, 1H), 7.25-7.35 (m, 2H), 12.92 (br. s., 1H).

Workup

  1. extractionextracted with 10% methanol/dichloromethane (3×50 mL)
  2. dry with materialThe combined organics were dried over sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-c0267803ca3e4ede8fda487e65759310
Source dataset
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07741327B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes