HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185751Generated: October 29, 2026
2-Methylbenzenesulfonic acid hydrate → HCID 21345163, compound
https://huagongshe.com/reaction/2185751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylbenzenesulfonic acid hydrate | HCID 12496995 | — |
| Reactant | HCID 21345162 | HCID 21345162 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21345163 | HCID 21345163 | 32.6% |
Reaction Steps
2,6-Difluoro-3-(1-Cbz-2-(S)-azetidinylmethoxy)pyridine from Example 116b (640 mg, 1.9 mmol) was combined with 10% Pd on C (50 mg) and p toluenesulfonic acid monohydrate (1.1 g, 5.7 mmole) in 30 mL of EtOH, and the mixture was stirred under an H2 atmosphere for 16 hours. The mixture was concentrated, triturated with ether and then recrystallized from ethyl acetate/ether to yield 231 mg (32.4%) of the title compound: mp 140-143° C. 1H NMR (D2O 300 MHz) δ: 2.40 (s, 3H), 2.69 (m, 2H), 4.12 (m, 2H), 4.46 (d, J=4.5, 2H), 4.94 (m, 1H), 7.01 (m, 1H), 7.38 (d,J=8.0, 2H), 7.70 (d,J=8.0, 2H), 7.81 (m, 1H). MS (DCI/NH3) m/e 201 (M+H)+, 218 (M+NH4)+. Anal. calcd. for C9H10F2N2O.C7H8O3S: C, 51.61; H, 4.87; N, 7.52. Found: C, 51.37; H, 4.89; N, 7.40. [α]D −1.44 (c 1, MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06403575B1 |
|---|
| Source dataset | uspto-grants-2002_06 |
|---|
| ORD ID | ord-fe1d00deb41142cc88836714c0e5b6a7 |
|---|
| Source note | uspto-grants-2002_06 |
|---|