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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794761Generated: November 4, 2026

Sodium Bicarbonate → HCID 44377804, compound

https://huagongshe.com/reaction/1794761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-[4-(4-Oxo-piperidin-1-yl)-benzyl]-thiazolidine-2,4-dioneHCID 12965955—
ReactantHCID 86584545HCID 86584545—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductHCID 44377804HCID 44377804—

Reaction Steps

To a stirred mixture of copper(II) sulfate pentahydrate (0.042 g, 0.17 mmol) in N,N-dimethylformamide (15 mL) was added sodium borohydride (0.037 g, 1 mmol). To the resulting suspension was added N-[5-((1R)-2-azido-1-hydroxy-ethyl)-2-chloro-phenyl]-methanesulfonamide (which was obtain in Example 25) (0.11 g, 0.38 mmol). After stirring for 20 minutes more copper(II) sulfate pentahydrate (0.042 g, 0.17 mmol) and sodium triacetoxyborohydride (0.064 g, 0.3 mmol) was added. The reaction mixture was stirred for 2.5 hours and then 5-[4-(4-oxo-piperidin-1-yl)-benzyl]-thiazolidine-2,4-dione (which was obtained in Example 38) (0.116 mg, 0.38 mmol), sodium triacetoxyborohydride (0.212 g, 1.0 mmol), and acetic acid (0.2 mL) were added. After stirring for 1.5 hours aqueous sodium bicarbonate solution was added and the resulting solid was collected. The product was purified by flash silica gel chromatography eluting with methylene chloride and methanol to give the title compound as a pale grey solid; mp>105° C. (decomposed); 1H NMR (300 MHz, DMSO-d6) δ 1.30–1.50(m, 2 H), 1.80–2.00(m, 2 H), 2.60–3.60(m, 9 H), 3.00(s, 3 H), 4.40–4.55(m, 1 H), 4.65–4.75(m, 1 H), 6.84(d, J=8.4 Hz, 2 H), 7.04(d, J=8.4 Hz, 1 H), 7.20(d, J=8.1 Hz, 1 H), 7.40–7.50(m, 2 H); MS (ES) m/z: 553.2 (MH+, 100%); HRMS Calcd. for C24H30ClN4O5S2 (MH+): 553.1440. Found: 553.1336.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022716B2
Source datasetuspto-grants-2006_04
ORD IDord-ee0bf0f10d3f4ea99b7470369d6740d3
Source noteuspto-grants-2006_04