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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76370Generated: October 29, 2026

Hydrochloric Acid → HCID 23650960, compound

https://huagongshe.com/reaction/76370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantSodium PyrosulfiteHCID 656671—
Reactant4-Fluoro-3-methylbenzene-1,2-diamineHCID 22055547—
Reactant4-Methyl-2-((3-(1-methylpiperidin-4-yl)propyl)amino)pyrimidine-5-carbaldehydeHCID 46221560—
SolventDimethylformamideHCID 6228—
ProductHCID 23650960HCID 23650960—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a 2 L Erlenmeyer flask were added 4-fluoro-3-methyl-benzene-1,2-diamine.HCl (46.32 g, 262.3 mmol), Na2S2O5 (64.82 g, 341.0 mmol), and 4-methyl-2-[3-(1-methyl-piperidin-4-yl)-propylamino]-pyrimidine-5-carbaldehyde (72.5 g, 262.3 mmol) in DMF (725 mL). To the resultant mixture was then added triethylamine (36.6 mL, 262.3 mmol), and the reaction was warmed on a hot plate with stirring to 90° C. and held at this temperature for 2 hours. The resultant mixture was then concentrated to near dryness and partitioned between dichloromethane (1 L) and 1 N NaOH (1 L). After separation of the layers, the aqueous layer was extracted a second time with dichloromethane (1 L). The combined organic layers were then washed with saturated aqueous NaHCO3 (1.6 L). The organics were then extracted with a 1 M mono/dibasic phosphate buffer (pH 5.62, 1.23 L). The aqueous layer was then basified with 50% NaOH (80 mL) to pH 10.8. The resultant heterogeneous layer was then extracted with dichloromethane (1.5 L and 500 mL), and the combined organics were concentrated to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835633B2
Source datasetuspto-grants-2014_09
ORD IDord-f76572d9538c405aade718cd1ea1ee32
Source noteuspto-grants-2014_09