Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185754Generated: October 29, 2026

p-Toluenesulfonic acid monohydrate → HCID 21345177, compound

https://huagongshe.com/reaction/2185754

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 21345174HCID 21345174—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 21345177HCID 2134517760.3%

Reaction Steps

2-Fluoro-6-methyl-3-(1-Cbz-2-(S)-azetidinylmethoxy)pyridine from Example 117d (714 mg, 2.16 mmol) was combined with 10% Pd/C (50 mg) and p-toluenesulfonic acid monohydrate (830 mg, 4.36 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 480 mg (60%) of the title compound. mp 141-143° C. 1H NMR (D2O 300 MHz) δ: 2.40 (s, 6H), 2.65-2.71 (m, 2H), 4.07-4.16 (m, 2H), 4.43(d, J=4.5, 2H), 4.81-95 (m, 1H), 7.16 (d, J=8.0, 1H), 7.37 (d,J=8.0, 2H), 7.55 (dd, J=8.0, 2.5, 1H), 7.70 (d,J=8.0, 2H). MS (DCI/NH3) m/e 197 (M+H)+ 214 (M+NH4)+. Anal. calcd. for C10H13FN2O.C7H8S: C, 55.42; H, 5.75; N, 7.60. Found: C, 55.27; H, 5.69; N, 7.44. [α]D −3.2 (c 1, MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403575B1
Source datasetuspto-grants-2002_06
ORD IDord-fe6d88397cc54135af1c0ceec71193ca
Source noteuspto-grants-2002_06