Hydrochloric Acid → HCID 178516629, 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]=[C:19]([F:21])[CH:18]=[C:17]([F:22])[C:16]=4[F:23])[C:13](=[O:24])[CH:12](C(OCC)=O)[C:11]3=[O:30])=[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]=[C:19]([F:21])[CH:18]=[C:17]([F:22])[C:16]=4[F:23])[C:13](=[O:24])[CH2:12][C:11]3=[O:30])=[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-(2,3,5-trifluorophenyl)pyrrolidine-3-carboxylate (which may be prepared in accordance with the procedure described for Intermediate 7; 0.036 g, 0.086 mmol) and 5 N aqueous hydrochloric acid (3 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-a806853ea01b49a8be8cd9cf6e314b77
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08530670B2
Reaction notes
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