Lithium Hydroxide → HCID 59732414, compound
Reaction equation
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[C:7]2[S:21][CH:20]=[CH:19][C:8]=2[N:9]=[C:10]([CH2:12][CH2:13][C:14]([O:16]CC)=[O:15])[N:11]=1.[OH-].[Li+]>C1COCC1.O>[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[C:7]2[S:21][CH:20]=[CH:19][C:8]=2[N:9]=[C:10]([CH2:12][CH2:13][C:14]([OH:16])=[O:15])[N:11]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of ethyl 3-(4-(2-furyl)thieno[3,2-d]pyrimidine-2-yl)propionate (0.07 g, 0.23 mmol) in THF (1.0 mL) and water (1.0 mL) was treated with lithium hydroxide (0.10 g, 2.32 mmol), stirred at room temperature for 16 h, concentrated in vacuo, dissolved in water, acidified to pH 2 by the addition of HCl (0.1 mL, 6.0-M), cooled in ice and filtered to give the title compound (0.052 g, 81%) as a white solid.
Workup
- concentrationconcentrated in vacuo
- dissolutiondissolved in water
- additionacidified to pH 2 by the addition of HCl (0.1 mL, 6.0-M)
- temperaturecooled in ice
- filtrationfiltered
Sources & evidence
- ORD record
- ord-a8fc51ad6b9f4432bd8745d5a15acd20
- Source dataset
- uspto-grants-2008_06
- Patent number
- US07384949B2
Reaction notes
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