Trifluoroacetic acid → HCID 58393372, compound
Reaction equation
[NH:1]1[C@@H:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C@H:4]2[NH:3][CH:2]1[C:10]1[CH:15]=[CH:14][C:13]([CH2:16][CH2:17][NH:18]C(=O)OC(C)(C)C)=[CH:12][CH:11]=1.C(O)(C(F)(F)F)=O>C(Cl)Cl>[NH:1]1[C@@H:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C@H:4]2[NH:3][CH:2]1[C:10]1[CH:11]=[CH:12][C:13]([CH2:16][CH2:17][NH2:18])=[CH:14][CH:15]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
tert-butyl (2-{4-[(3aR,7aR)-octahydro-1H-benzimidazol-2-yl]phenyl}ethyl)carbamate (50 mg, 0.15 mmol) was stirred in a 4:1 mixture of DCM:TFA (1 mL) at ambient temperature for 18 h. The reaction was concentrated in vacuo and the crude product used without further purification.
Workup
- concentrationThe reaction was concentrated in vacuo
- customthe crude product used without further purification
Sources & evidence
- ORD record
- ord-0f462ca0f42e4e428b660eb1b2bed395
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08623859B2
Reaction notes
Loading…