HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208682Generated: October 30, 2026
Trifluoroacetic acid → HCID 66575763, compound
https://huagongshe.com/reaction/2208682
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 4-((5-bromo-3-(((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl) methyl)carbamoyl)-2-methylphenyl)(methyl)amino)piperidin-1-carboxylate | HCID 70872376 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66575763 | HCID 66575763 | 85% |
Reaction Steps
A stirred solution of tert-butyl 4-((5-bromo-3-(((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)carbamoyl)-2-methylphenyl)(methyl)amino)piperidin-1-carboxylate (1.3 g, 2.39 mmol) in DCM (10 mL) was cooled to 0° C. and TFA (2 mL) was added to it. Reaction mass was stirred at room temperature for 1 h. On completion, reaction was concentrated to dryness. Residue was basified with aqueous sodium bicarbonate till pH 8 and aqueous layer extracted with 20% MeOH/DCM. Combined organic layers were dried over sodium sulfate and concentrated to afford the desired compound (0.9 g, 85%). LCMS: 461.15 (M+1)+; HPLC: 98.52% (@ 254 nm) (Rt; 4.673; Method: Column: YMC ODS-A 150 mm×4.6 mm×5μ; Mobile Phase: A; 0.05% TFA in water/B; 0.05% TFA in acetonitrile; Inj. Vol: 10 μL, Col. Temp.: 30° C.; Flow rate: 1.4 mL/min.; Gradient: 5% B to 95% B in 8 min, Hold for 1.5 min, 9.51-12 min 5% B); 1H NMR (DMSO-d6, 400 MHz) δ 8.22 (t, 1H), 7.19 (s, 1H), 7.01 (s, 1H), 5.85 (s, 1H), 4.23 (d, 2H, J=4 Hz), 2.91 (d, 2H, J=11.6 Hz), 2.78 (bs, 1H), 2.55 (s, 3H), 2.32-2.35 (m, 2H), 2.18 (s, 3H), 2.10 (s, 6H), 1.44-1.50 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376422B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-353781b6b6494115a26da6783d13f351 |
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| Source note | uspto-grants-2016_06 |
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