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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786962Generated: October 30, 2026

Sodium Bicarbonate → HCID 57597211, compound

https://huagongshe.com/reaction/1786962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthanamine, 2-(methylsulfonyl)-, hydrochloride (1:1)HCID 17749886—
ReactantHCID 86615765HCID 86615765—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductHCID 57597211HCID 5759721171.4%

Reaction Steps

To a solution of 4-[7-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-2H-pyrazolo[4,3-d]pyrimidin-2-yl]benzaldehyde (80 mg) and 2-(methylsulfonyl)ethylamine hydrochloride (40 mg) in N,N-dimethylformamide (2 mL) was added acetic acid (0.02 mL), and the mixture was stirred at room temperature for 1 hr. Subsequently, sodium triacetoxyborohydride (54 mg) was added, and the mixture was stirred at the same temperature for 2 hrs. After the completion of the reaction, saturated aqueous sodium hydrogen carbonate was added, and the mixture was concentrated under reduced pressure. The residue was extracted with ethyl acetate, and the organic layer washed with water and saturated brine and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate/methanol=5/1) to give the title compound (70 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507740B2
Source datasetuspto-grants-2009_03
ORD IDord-3d6e77701d014150b9dbb8d685c09bbe
Source noteuspto-grants-2009_03