Hydrochloric Acid → 3-[5-Fluoro-3-(tetrahydro-pyran-4-yl)-pyridin-2-yloxy]-cyclobutanecarboxylic acid

HRID 1846788Notes

Reaction equation

C[O:2][C:3]([CH:5]1[CH2:8][CH:7]([O:9][C:10]2[C:15]([CH:16]3[CH2:21][CH2:20][O:19][CH2:18][CH2:17]3)=[CH:14][C:13]([F:22])=[CH:12][N:11]=2)[CH2:6]1)=[O:4].[OH-].[Li+].Cl>CO.O>[F:22][C:13]1[CH:14]=[C:15]([CH:16]2[CH2:21][CH2:20][O:19][CH2:18][CH2:17]2)[C:10]([O:9][CH:7]2[CH2:8][CH:5]([C:3]([OH:4])=[O:2])[CH2:6]2)=[N:11][CH:12]=1

Participants

Conditions

Temperature: 50 °C

Procedure

To a solution of 3-[5-fluoro-3-(tetrahydro-pyran-4-yl)-pyridin-2-yloxy]-cyclobutanecarboxylic acid methyl ester (3.2 g) in MeOH (60 mL) and water (15 mL) at RT was added lithium hydroxide (1.0 g, 41.6 mmol). The reaction mixture was heated to 50° C. for 2 h and then additional LiOH (400 mg) was added. Stirring was continued at 50° C. for 1 h. The reaction was neutralized with 5 M HCl and concentrated. The concentrated solution was extracted with EtOAc (50 mL) and the organic layer was washed with water (10 mL), brine (10 mL), dried over MgSO4 and concentrated to give the product (1.5 g), which was used in the next step without further purification.

Workup

concentrationconcentrated
extractionThe concentrated solution was extracted with EtOAc (50 mL)
washthe organic layer was washed with water (10 mL), brine (10 mL)
dry with materialdried over MgSO4
concentrationconcentrated

Sources & evidence

ORD record: ord-974c1f8d1a8f4ec4adaea663d773b8e7
Source dataset: uspto-grants-2015_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08952037B2

Reaction notes

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