Hydrochloric Acid → HCID 68432311, compound
Reaction equation
[Cl:1][C:2]1[C:7](=[O:8])[N:6]([CH2:9][C:10]([NH:12][CH:13]([CH2:19][CH3:20])[C:14]([O:16]CC)=[O:15])=[O:11])[N:5]=[CH:4][C:3]=1[NH:21][C@@H:22]1[CH2:27][C@@H:26]2[CH2:28][C@@H:24]([C:25]2([CH3:30])[CH3:29])[C@H:23]1[CH3:31].[OH-].[Na+].Cl>O1CCOCC1>[Cl:1][C:2]1[C:7](=[O:8])[N:6]([CH2:9][C:10]([NH:12][CH:13]([CH2:19][CH3:20])[C:14]([OH:16])=[O:15])=[O:11])[N:5]=[CH:4][C:3]=1[NH:21][C@@H:22]1[CH2:27][C@@H:26]2[CH2:28][C@@H:24]([C:25]2([CH3:29])[CH3:30])[C@H:23]1[CH3:31]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 2-({[5-chloro-6-oxo-4-{[(1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]amino}pyridazin-1(6H)-yl]acetyl}amino)butyrate (64 mg, 0.145 mmol) in 1,4-dioxane (2 mL) was stirred with 1 M aqueous sodium hydroxide (435 μL, 0.435 mmol) at room temperature for 2 hours. After completion of the reaction, the reaction solution was neutralized with 1 M hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and evaporated under reduced pressure to give the desired product.
Workup
- customAfter completion of the reaction
- extractionextracted with ethyl acetate
- dry with materialThe extract was dried over anhydrous magnesium sulfate
- customevaporated under reduced pressure
Sources & evidence
- ORD record
- ord-55dd884ca9094ce9a228d6d23796c7dd
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08440666B2
Reaction notes
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