HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423692Generated: October 31, 2026
Trifluoroacetic acid → 2-[4-(Methylsulfonyl)phenyl]-5-(4-piperidinylmethoxy)pyridine
https://huagongshe.com/reaction/423692
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1,1-Dimethylethyl 4-[({6-[4-(methylsulfonyl)phenyl]-3-pyridinyl}oxy)methyl]-1-piperidinecarboxylate | HCID 24994333 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[4-(Methylsulfonyl)phenyl]-5-(4-piperidinylmethoxy)pyridine | HCID 59718586 | 84% |
Reaction Steps
TFA (2 mL) was added to a solution of 1,1-dimethylethyl 4-[({6-[4-(methylsulfonyl)phenyl]-3-pyridinyl}oxy)methyl]-1-piperidinecarboxylate (705 mg, 1.58 mmol) in CH2Cl2 (50 mL) at ambient temperature. The mixture was stirred at ambient temperature overnight. The mixture was concentrated, and the crude product was purified by chromatography on a silica gel column using 0 to 10% MeOH/CH2Cl2 give 460 mg (84%) of 2-[4-(methylsulfonyl)phenyl]-5-[(4-piperidinylmethyl)oxy]pyridine as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 8.44 (d, 1H, J=2.9 Hz), 8.29 (d, 2H, J=8.6 Hz), 8.08 (d, 1H, J=8.8 Hz), 8.00 (d, 2H, J=8.6 Hz), 7.55 (dd, 1H, Ja=8.8 Hz, Jb=3.0 Hz), 4.04 (d, 2H, J=6.2 Hz), 3.40-3.25 (m, 2H), 3.25 (s, 3H), 3.01-2.83 (m, 2H), 2.22-2.02 (m, 1H), 2.00-1.90 (m, 2H), 1.60-1.37 (m, 2H); LRMS (ESI), m/z 347 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101634B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-0d5158fe730644ef896a5917925bedec |
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| Source note | uspto-grants-2012_01 |
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