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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509915Generated: November 3, 2026

Diisopropylethylamine → HCID 117856350, compound

https://huagongshe.com/reaction/509915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3,5-Diamino-6-chloro-pyrazine acidHCID 6452119—
ReactantHCID 131733252HCID 131733252—
SolventDimethylformamideHCID 6228—
ProductHCID 117856350HCID 117856350—

Reaction Steps

A solution of 3,5-diamino-6-chloropyrazine-2-carboxylic-acid (Intermediate 1.1.1, 46 mg, 0.25 mmol), 3-amino-1-ethoxycarbonylmethyl-1-[3-(4-methoxy-phenyl)-propyl]-piperidinium bromide trifluoroacetate salt (Intermediate 3.1.2, 230 mg, 0.25 mmol), O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (86 mg, 0.27 mmol) and N,N-diisopropylethylamine (0.15 mL, 0.1 mmol) in dry N,N-dimethylformamide (5 mL) is stirred for 5 hours at room temperature. The solution is concentrated under reduced pressure to half of the volume, water (2 mL) added and the mixture purified via preparative reverse phase HPLC (gradient of acetonitrile in water+0.05% trifluoroacetic acid). Fractions containing the title compound are concentrated under reduced pressure. The residue is treated with HCl in diethyl ether (2 M, 2 mL), the solvent removed and the residue dried at 50° C. under vacuum. Yield: 56 mg. IC50=0.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096548B2
Source datasetuspto-grants-2015_08
ORD IDord-a3a5e5c9a2dd48328160d8f249c6d336
Source noteuspto-grants-2015_08