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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814868Generated: November 1, 2026

Formaldehyde → HCID 10173268, compound

https://huagongshe.com/reaction/1814868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 22498748HCID 22498748—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 10173268HCID 1017326858.2%

Reaction Steps

Aq. formaldehyde (0.19 mL) and sodium triacetoxy borohydride (0.526 g) were added to a suspension of N-(4-chlorobenzyl)-2-(((2-hydroxypropyl)-amino)methyl)-7-methyl-4-oxo-4,7-dihydrofuro[2,3-b]pyridine-5-carboxamide (Example 33, 0.500 g) in],2-dichloroethane (50 mL). The reaction mixture was stirred at room temperature for 18 h. A sat. aq. sodium bicarbonate solution (30 mL) was added. The aqueous layer was separated and extracted with CH2Cl2 (4×50 mL). The combined organic layers were dried (MgSO4), filtered, and concentrated in vacuo. The resulting solid was purified by column chromatography (CH2Cl2/methanol; 97/3, 96/4) followed by recrystallization from ethyl acetate to yield 0.301 g of the title compound as a white solid. Physical characteristics. M.p. 152° C.; 1H NMR (400 MHz, DMSO-d6) δ 10.65, 8.55, 7.41-7.32, 6.87, 4.55, 4.35, 3.92, 3.80-3.73, 3.69, 2.36-2.31, 2.28-2.20, 1.04; MS (EST+) m/z 418 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878705B2
Source datasetuspto-grants-2005_04
ORD IDord-1dcf35d2eae549d19ca991287261be72
Source noteuspto-grants-2005_04