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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367084Generated: October 31, 2026

2-Methylbenzenesulfonic acid hydrate → HCID 21345163, compound

https://huagongshe.com/reaction/367084

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzenesulfonic acid hydrateHCID 12496995—
ReactantHCID 21345162HCID 21345162—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 21345163HCID 2134516332.6%

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) 6: 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, 51.61H, 4.87 N, 7.52 Found: C, 51.37 H, 4.89; N, 7.40. [α]D -1.44 (c 1, MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133253
Source datasetuspto-grants-2000_10
ORD IDord-2ad5dc2b84424a54bfe5826689db2a1c
Source noteuspto-grants-2000_10