HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185755Generated: October 30, 2026
2-Methylbenzenesulfonic acid hydrate → HCID 21345175, compound
https://huagongshe.com/reaction/2185755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylbenzenesulfonic acid hydrate | HCID 12496995 | — |
| Reactant | HCID 21345173 | HCID 21345173 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21345175 | HCID 21345175 | 50% |
Reaction Steps
2-Fluoro-6-methyl-3-(1-Cbz-2-(R)-azetidinylmethoxy)pyridine from step 118a (500 mg, 1.51 mmol) was combined with 10% Pd/C (50 mg) and p toluenesulfonic acid monohydrate (600 mg, 3.15 mmole) in 30 mL of EtOH, and the mixture was stirred under an H2 atmosphere for 16 hours. The mixture was filtered, concentrated, the residue was triturated with ether, and the product was recrystallized from ethyl acetate/ether to yield 270 mg (50%) of the title compound. mp 158-160° C. 1H NMR (D2O 300 MHz) δ2.40 (s, 6H), 2.65-2.70 (m, 2H), 4.07-4.18 (m, 2H), 4.42 (d, J=4.5, 2H), 4.91-95 (m, 1H), 7.15 (d, J=8.0, 1H), 7.37 (d,J=8.0, 2H), 7.55 (dd, J=8.0, 2.0, 1H), 7.69 (d,J=8.5, 2H). MS (DCI/NH3) m/e 197 (M+H)+ 214 (M+NH4)+. Anal. calcd. for C10H13FN2O.C7H8O3S.0.4 H2O: C, 54.36; H, 5.85; N, 7.46. Found: C, 54.48; H, 5.81; N, 7.28; [α]D +2.05 (c 1, MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06403575B1 |
|---|
| Source dataset | uspto-grants-2002_06 |
|---|
| ORD ID | ord-d01da9b737b6450abc8401fae858f825 |
|---|
| Source note | uspto-grants-2002_06 |
|---|