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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341469Generated: October 25, 2026

Acetonitrile → HCID 66802658, compound

https://huagongshe.com/reaction/341469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant6-Chloro-N2-methyl-N2-(phenylmethyl)-1,3,5-triazine-2,4-diamineHCID 56831790—
CatalystTetrabutylammonium CyanideHCID 165872—
SolventEthyl AcetateHCID 8857—
ProductHCID 66802658HCID 66802658—

Reaction Steps

To N-Benzyl-6-chloro-N-methyl-[1,3,5]triazine-2,4-diamine (Intermediate 34, 350 mg, 1.40 mmol) was added tetra n-butylammonium cyanide (1.15 g, 4.28 mmol) and anhydrous acetonitrile (15 mL). The reaction mixture was stirred at 50 C for 1 h, diluted with EtOAc (20 mL), extracted with water (2×10 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to furnish the desired product, which was used directly without further purification (327 mg, 97%). Method C HPLC-MS: MH+ requires m/z=241. Found: m/z=241, Rt=1.29 min (86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895733B2
Source datasetuspto-grants-2014_11
ORD IDord-c6704323257b433fa57dc790b9103f38
Source noteuspto-grants-2014_11