Ammonium Chloride → HCID 59128868, compound
Reaction equation
[C:1]([C:5]1[CH:32]=[CH:31][CH:30]=[CH:29][C:6]=1[O:7][C:8]1[C:13]([NH:14][C:15]2[S:19][C:18]([C:20]([CH3:28])([CH3:27])[CH2:21][CH2:22][C:23]([O:25]C)=[O:24])=[N:17][N:16]=2)=[CH:12][CH:11]=[CH:10][N:9]=1)([CH3:4])([CH3:3])[CH3:2].O.[OH-].[Li+].[Cl-].[NH4+]>C1COCC1.O>[C:1]([C:5]1[CH:32]=[CH:31][CH:30]=[CH:29][C:6]=1[O:7][C:8]1[C:13]([NH:14][C:15]2[S:19][C:18]([C:20]([CH3:27])([CH3:28])[CH2:21][CH2:22][C:23]([OH:25])=[O:24])=[N:17][N:16]=2)=[CH:12][CH:11]=[CH:10][N:9]=1)([CH3:2])([CH3:3])[CH3:4]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of methyl 4-(5-(2-(2-tert-butylphenoxy)pyridin-3-ylamino)-1,3,4-thiadiazol-2-yl)-4-methylpentanoate (Example 96) (450 mg, 1.0 mmol), lithium hydroxide hydrate (125 mg, 3 mmol) in THF (10 mL) and water (2 mL) was stirred at rt for 2 h. A solution of saturated ammonium chloride was added and mixture was extracted twice using ethyl acetate. The organic phase was separated, dried (MgSO4), filtered and evaporated. The crude material was purified by preparative HPLC to give the title compound (430 mg, TFA salt) as a white solid. (M+H)+=441.
Workup
- extractionmixture was extracted twice using ethyl acetate
- customThe organic phase was separated
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated
- customThe crude material was purified by preparative HPLC
Sources & evidence
- ORD record
- ord-2596c700500f42aeb3c778eea405824c
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07645778B2
Reaction notes
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