Trifluoroacetic acid → HCID 67336664, compound
Reaction equation
C(C(O)=O)(F)(F)F.[O:8]=[C:9]1[N:13](C(OC(C)(C)C)=O)[C:12]2[CH:21]=[CH:22][CH:23]=[CH:24][C:11]=2[N:10]1[CH:25]1[CH2:30][CH2:29][S:28][CH2:27][CH2:26]1>C(Cl)Cl>[S:28]1[CH2:27][CH2:26][CH:25]([N:10]2[C:11]3[CH:24]=[CH:23][CH:22]=[CH:21][C:12]=3[NH:13][C:9]2=[O:8])[CH2:30][CH2:29]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
CF3CO2H (1 mL) was added to a solution of tert-butyl 2-oxo-3-tetrahydro-2H-thiopyran-4-yl-2,3-dihydro-1H-benzimidazole-1-carboxylate from Step A (210 mg, 0.628 mmol) in CH2Cl2 (3 mL). After 2 h, the mixture was concentrated in vacuo to give the title compound. MS: m/z=235 (M+1).
Workup
- concentrationthe mixture was concentrated in vacuo
Sources & evidence
- ORD record
- ord-eadad0323e23455bbf55d66393cba06c
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08173655B2
Reaction notes
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