Hydrochloric Acid → HCID 67975417, compound
Reaction equation
C(OC([N:8]1[C:12](=[O:13])/[C:11](=[CH:14]\N(C)C)/[CH:10]2[CH2:18][C:19]3[C:24]([CH:9]12)=[CH:23][CH:22]=[CH:21][CH:20]=3)=O)(C)(C)C.Cl.[O:26]1CCOCC1>O>[OH:26]/[CH:14]=[C:11]1/[CH:10]2[CH2:18][C:19]3[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH:9]2[NH:8][C:12]/1=[O:13]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 3-[1-dimethylamino-meth-(Z)-ylidene]-2-oxo-3,3a,4,8b-tetrahydro-2H-indeno[1,2-b]pyrrole-1-carboxylic acid tert-butyl ester D1 (1.68 g, 4.63 mmol) in dioxane (50 mL) was added HCl (37%, 8.37 mL). The solution was stirred overnight at room temperature and was then diluted with water, extracted with ethyl acetate, washed with brine, dried and concentrated to give 3-[1-Hydroxy-meth-(Z)-ylidene]-3,3a,4,8b-tetrahydro-1H-indeno[1,2-b]pyrrol-2-one C1 identical to method A (0.85 g, 78%).
Workup
- extractionextracted with ethyl acetate
- washwashed with brine
- customdried
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-df8b2b1e4bdf42b6874e90a0cd8b676c
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946280B2
Reaction notes
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