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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905695Generated: October 31, 2026

Formaldehyde → HCID 67389135, compound

https://huagongshe.com/reaction/905695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantDimethylformamideHCID 6228—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 67388260HCID 67388260—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
SolventEthylacetate methanolHCID 21584119—
ProductHCID 67389135HCID 67389135—

Reaction Steps

A 7 ml portion of DMF solution containing 685 mg of 2-{[4-(aminomethyl)phenyl]amino}-4-[(3-methylphenyl)amino]pyrimidine-5-carboxamide dihydrochloride was mixed with 0.45 ml of triethylamine, 420 mg of 35% aqueous formalin and 1.09 g of sodium triacetoxy borohydride, followed by stirring overnight at room temperature. The reaction mixture was mixed with water, concentrated and then purified by a silica gel column chromatography (chloroform:methanol:aqueous ammonia) to obtain crude crystals. This was dissolved in a methanol-ethyl acetate mixed solution and mixed with 1 ml of 4 M hydrogen chloride/ethyl acetate solution, and the thus precipitated crystals were collected by filtration and further recrystallized (methanol-water) to obtain 164 mg of 2-({4-[(dimethylamino)methyl]phenyl}amino)-4-[(3-methylphenyl)amino]pyrimidine-5-carboxamide dihydrochloride as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012959B2
Source datasetuspto-grants-2011_09
ORD IDord-ba375c454ea843a0960aa6d7ec73c257
Source noteuspto-grants-2011_09