Lithium Hydroxide → HCID 66844822, compound
Reaction equation
[C:1]1([C@H:7]([NH:9][C:10]([N:12]2[CH2:17][CH:16]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH2:15][CH:14]([C:24]([O:26]C)=[O:25])[CH2:13]2)=[O:11])[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Li+].[OH-]>C1COCC1.CO>[C:1]1([C@H:7]([NH:9][C:10]([N:12]2[CH2:17][CH:16]([C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)[CH2:15][CH:14]([C:24]([OH:26])=[O:25])[CH2:13]2)=[O:11])[CH3:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a 150 mL RBF was added the mixture from step 1 (150 mg), THF:MeOH (3:1, 15 mL), and LiOH, 1M (1.00 ml, 1.0 mmol) and the mixture was stirred at RT. After 2 hours, the reaction was neutralized and extracted with EtOAc (3×20 mL). The combined organic layers were concentrated in vacuo to give a white solid. The material was carried forward without further purification.
Workup
- extractionextracted with EtOAc (3×20 mL)
- concentrationThe combined organic layers were concentrated in vacuo
- customto give a white solid
- customThe material was carried forward without further purification
Sources & evidence
- ORD record
- ord-1707480d73ac4e1ab4bf71d7028004fe
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07872009B2
Reaction notes
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