Hydrochloric Acid → HCID 69267676, compound
Reaction equation
[O:1]1[C:5]2[C:6]([C:10]3[C:11](=[O:36])[NH:12][C:13](=[O:35])[C:14]=3[C:15]3[C:23]4[C:18](=[CH:19][CH:20]=[CH:21][C:22]=4F)[N:17]([CH:25]4[CH2:34][CH2:33][C:28]5(OCC[O:29]5)[CH2:27][CH2:26]4)[CH:16]=3)=[CH:7][CH:8]=[CH:9][C:4]=2[CH:3]=[CH:2]1.Cl>O1CCCC1>[O:1]1[C:5]2[C:6]([C:10]3[C:11](=[O:36])[NH:12][C:13](=[O:35])[C:14]=3[C:15]3[C:23]4[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=4)[N:17]([CH:25]4[CH2:34][CH2:33][C:28](=[O:29])[CH2:27][CH2:26]4)[CH:16]=3)=[CH:7][CH:8]=[CH:9][C:4]=2[CH:3]=[CH:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Dissolve 3-(Benzofur-7-yl)-4-[1-(1,4-dioxa-spiro[4.5]dec-8-yl)-4-fluoro-1H-indol-3-yl]pyrrole-2,5-dione (1.40 g, 2.88 mmol) in tetrahydrofuran (20 mL) and stir at room temperature. Add 1N hydrochloric acid (20 mL) and heat the reaction to reflux for 24 h. Upon completion, Filter the product, rinse with cold water, and dry under vaccuum. The orange solid is used without further purification, 1.1 g (87%). MS (ES, m/z): 443.18(M++1), 441.13(M+−1).
Workup
- temperatureheat
- customthe reaction
- temperatureto reflux for 24 h
- filtrationUpon completion, Filter the product
- washrinse with cold water
- customdry under vaccuum
- customThe orange solid is used without further purification, 1.1 g (87%)
Sources & evidence
- ORD record
- ord-6fa3d86853054960ba477965743f444c
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07405305B2
Reaction notes
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