Potassium Hydroxide → HCID 59589749, compound
Reaction equation
C([O:3][C:4](=[O:35])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]2[N:16]3[N:17]=[C:18]([NH:20][C:21]4[CH:26]=[CH:25][C:24]([O:27][CH2:28][CH2:29][N:30]5[CH2:34][CH2:33][CH2:32][CH2:31]5)=[CH:23][CH:22]=4)[N:19]=[C:15]3[CH:14]=[CH:13][CH:12]=2)[CH:6]=1)C.[OH-].[K+]>C(O)C>[N:30]1([CH2:29][CH2:28][O:27][C:24]2[CH:25]=[CH:26][C:21]([NH:20][C:18]3[N:19]=[C:15]4[CH:14]=[CH:13][CH:12]=[C:11]([C:7]5[CH:6]=[C:5]([CH:10]=[CH:9][CH:8]=5)[C:4]([OH:35])=[O:3])[N:16]4[N:17]=3)=[CH:22][CH:23]=2)[CH2:31][CH2:32][CH2:33][CH2:34]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-{2-[4-(2-Pyrrolidin-1-yl-ethoxy)-phenylamino]-[1,2,4]triazolo[1,5-a]pyridin-5-yl}-benzoic acid ethyl ester (1.28 g, 2.71 mmol) was dissolved in ethanol (20 ml) and potassium hydroxide (0.45 g, 8.12 mmol) was added. The reaction was heated to reflux for 3 hrs. Upon cooling the solvent was removed in vacuo and aqueous sodium hydrogencarbonate added to the residue. The basic aqueous layer was washed with dichloromethane, then neutralised with 2M HCl and the resulting precipitate collected by filtration, washed with water and toluene, then dried under vacuum to give the desired product. Yield: 0.64 g, 53%. LCMS RT: 2.45 min, MI: 444, Method: 2.
Workup
- temperatureThe reaction was heated
- temperatureto reflux for 3 hrs
- temperatureUpon cooling the solvent
- customwas removed in vacuo and aqueous sodium hydrogencarbonate
- additionadded to the residue
- washThe basic aqueous layer was washed with dichloromethane
- filtrationthe resulting precipitate collected by filtration
- washwashed with water and toluene
- customdried under vacuum
Sources & evidence
- ORD record
- ord-31fe72a0670a48bdad8f6e8ba58192eb
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09012633B2
Reaction notes
Loading…