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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710173Generated: November 4, 2026

D-Psicose → HCID 71257244, compound

https://huagongshe.com/reaction/710173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantD-PsicoseHCID 441036—
ReactantHCID 71257270HCID 71257270—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventHCID 178418361HCID 178418361—
ProductHCID 71257244HCID 7125724467.7%

Reaction Steps

Following the general procedure-1 Tert-butyl 4-{7-fluoro-2-[2-fluoro-4-(methylsulfonyl)phenyl]benzo[d]oxazol-5-yl}-5,6-dihydropyridine-1(2H)-carboxylate (180 mg) obtained from intermediate 31 (600 mg, 1.38 mmol) and tert-butyl 4-(trifluoromethylsulfonyloxy)-5,6-dihydropyridine-1(2H)-carboxylate (456 mg, 1.38 mmol). Tert-butyl 4-{7-fluoro-2-[2-fluoro-4-(methylsulfonyl)phenyl]benzo[d]oxazol-5-yl}-5,6-dihydropyridine-1(2H)-carboxylate (150 mg, 0.30 mmol) dissolved in MeOH and added Pd/C (71 mg). This mixture was stirred in an auto clave in hydrogen atmosphere at 55 Psi for 12 h. Reaction mixture filtered through celite and washed the cetile with MeOH. Methanol was removed on rotavapour to obtain the titled compound (100 mg) as a brown solid. M.P.: 188-192.4° C. 1H-NMR (δ ppm, CDCl3, 400 MHz): 8.47 (t, J 7.12, 1H), 7.89 (t, J 7.6, 2H), 7.49 (s, 1H), 7.07 (d, J 11.2, 1H), 4.28 (bs, 2H), 3.13 (s, 3H), 2.90-2.72 (m, 3H), 1.95-1.85 (m, 2H), 1.72-1.56 (m, 2H). 1.49 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181214B2
Source datasetuspto-grants-2015_11
ORD IDord-f48730b1e50640e5a6d30c982f8f92df
Source noteuspto-grants-2015_11