Hydrochloric Acid → HCID 178516626, compound
Reaction equation
[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([N:10]3[CH:14]([C:15]4[CH:20]=[CH:19][C:18]([N:21]5[CH2:26][CH2:25][O:24][CH2:23][CH2:22]5)=[CH:17][CH:16]=4)[C:13](=[O:27])[CH:12](C(OCC)=O)[C:11]3=[O:33])=[CH:9][C:4]=2[N:3]=[CH:2]1.Cl>>[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([N:10]3[CH:14]([C:15]4[CH:20]=[CH:19][C:18]([N:21]5[CH2:22][CH2:23][O:24][CH2:25][CH2:26]5)=[CH:17][CH:16]=4)[C:13](=[O:27])[CH2:12][C:11]3=[O:33])=[CH:9][C:4]=2[N:3]=[CH:2]1Participants
3
Procedure
The compound was synthesized starting from ethyl 1-(1H-benzo[d]imidazol-5-yl)-5-(4-morpholinophenyl)-2,4-dioxo-pyrrolidine-3-carboxylate (which may be prepared in accordance with the procedure described for Intermediate 8; 0.12 g, 0.2676 mmol) and 5 N aqueous hydrochloric acid (6 ml) according to the method described in Method 1, step 3.
Workup
- customThe compound was synthesized
- custommay be prepared in accordance with the procedure
Sources & evidence
- ORD record
- ord-81c5129b7510477c802ec24209b6b9c2
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08530670B2
Reaction notes
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