Trifluoroacetic acid → HCID 67442071, compound
Reaction equation
C(O)(C(F)(F)F)=O.[C:8](=[O:85])([O:17][C@H:18]1[C@:22]([F:24])([CH3:23])[C@H:21]([N:25]2[CH:33]=[N:32][C:31]3[C:26]2=[N:27][C:28]([NH:36]C(C2C=CC(OC)=CC=2)(C2C=CC(OC)=CC=2)C2C=CC=CC=2)=[N:29][C:30]=3[O:34][CH3:35])[O:20][C@@H:19]1[CH2:60][O:61]C(C1C=CC(OC)=CC=1)(C1C=CC(OC)=CC=1)C1C=CC=CC=1)[O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C([O-])(O)=O.[Na+]>C(Cl)Cl>[C:8](=[O:85])([O:9][CH2:10][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[O:17][C@H:18]1[C@:22]([F:24])([CH3:23])[C@H:21]([N:25]2[CH:33]=[N:32][C:31]3[C:26]2=[N:27][C:28]([NH2:36])=[N:29][C:30]=3[O:34][CH3:35])[O:20][C@@H:19]1[CH2:60][OH:61]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A 1 vol % of TFA solution in DCM (50 mL) was added to a flask loaded with 4 (2.69 g, 2.56 mmol). The mixture was stirred at room temperature for 2 h and it was complete. Sat. NaHCO3 (20 mL) was added and the mixture was partitioned in water and DCM. The organic layer was concentrated and solid residue was purified by column chromatography (silica gel, 0˜5% 2-PrOH in DCM) to afford 1.01 g of product, 5, as a white foam solid (yield 88%). 1H-NMR (CDCl3): δ 7.82 (s, 1H), 7.39-7.33 (m, 5H), 6.02 (d, 1H, J=19.2 Hz), 5.77 (dd, 1H, J=20.8, 8.8 Hz), 5.32-5.30 (m, 1H), 5.20 (s, 2H), 5.04 (s, 2H), 4.34 (d, 1H, J=8.8 Hz), 4.15 (m, 1H), 4.04 (s, 3H), 3.85-3.79 (m, 1H), 1.21 (d, 3H, J=22.8 Hz).
Workup
- customthe mixture was partitioned in water
- concentrationThe organic layer was concentrated
- customsolid residue was purified by column chromatography (silica gel, 0˜5% 2-PrOH in DCM)
Sources & evidence
- ORD record
- ord-c6162b8ac6f94330afd19039284841ac
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08563530B2
Reaction notes
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