Hydrochloric Acid → HCID 178516619, 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][CH:18]=[CH:17][CH:16]=4)[C:13](=[O:21])[CH:12](C(OCC)=O)[C:11]3=[O:27])=[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][CH:18]=[CH:17][CH:16]=4)[C:13](=[O:21])[CH2:12][C:11]3=[O:27])=[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)-2,4-dioxo-5-phenylpyrrolidine-3-carboxylate (which may be prepared in accordance with the procedure described for Intermediate 5; 0.1 g, 0.196 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-ef83aa774eb245a8ba28fbee97ea7e11
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08530670B2
Reaction notes
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