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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559084Generated: October 30, 2026

Acetonitrile → HCID 24894758, compound

https://huagongshe.com/reaction/559084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 66653069HCID 66653069—
ReactantHCID 74338134HCID 74338134—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
ProductHCID 24894758HCID 24894758—

Reaction Conditions

Temperature150 °C

Reaction Steps

6-Chloro-N-[1-naphthalen-2-yl-ethyl]-[1,3,5]triazine-2,4-diamine (30 mg, 0.1 mmol), 2-boc-protected amino-3-{3-[4,4,5,5,-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrazol-1-yl]-propionic acid (50 mg, 0.15 mmol), 1 ml of acetonitrile, and 0.7 ml of water. Aqueous sodium carbonate (0.3 ml and 1N) was added to a microwave vial, followed by 5 mol percent of dichlorobis(triphenylphosphine)-palladium(II). The reaction vessel was sealed and heated to 150° C. for 5 minutes with microwave. After cooling, the reaction mixture was evaporated to dryness, the residue was dissolved in 2.5 ml of methanol, and then was purified with Prep-LC to give 6.8 mg of boc protected 2-amino-3-{3-[4-amino-6-(1-naphthalen-2-yl-ethylamino)[1,3,5]triazin-2-yl]-pyrazol-1-yl}proionic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063057B2
Source datasetuspto-grants-2011_11
ORD IDord-e2af9ddbdb3e40cc8f17a9e33aa4bc88
Source noteuspto-grants-2011_11