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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351245Generated: October 30, 2026

Formaldehyde → HCID 21091081, compound

https://huagongshe.com/reaction/351245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 21091065HCID 21091065—
SolventMethanolHCID 887—
ProductHCID 21091081HCID 21091081—

Reaction Steps

37% aqueous solution of formaldehyde (0.23 ml) and sodium cyanoborohydride (53 mg) were added to a solution of N-(2-{4-[3-amino-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]-phenoxy}ethyl)urea (103.1 mg) in MeOH (2 ml). The reaction mixture was stirred at ambient temperature for 3 hours. 37% aqueous solution of formaldehyde (0.23 ml) and sodium cyanoborohydride (53 mg) were added to the mixture and the reaction mixture was stirred at ambient temperature for 4 days. The mixture was concentrated in vacuo, and the residue was partitioned between ethyl acetate and H2O. The organic layer was washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by preparative thin layer silica gel chromatography developed by CHCl3:MeOH:28% aqueous NH4OH=100:10:1. The separated silica gel was extracted with same solvent and the solvent was evaporated in vacuo to give N-(2-{4-[3-(dimethylamino)-1-(4-methoxyphenyl)-1-H-pyrazol-5-yl]phenoxy}ethyl)urea (59.9 mg) as an amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183306B2
Source datasetuspto-grants-2007_02
ORD IDord-86fa22e2c8084ed1b32c007265196ce6
Source noteuspto-grants-2007_02