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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364569Generated: October 29, 2026

Dimethylacetamide → HCID 178467439, compound

https://huagongshe.com/reaction/1364569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant4-Amino-5-cyano-6-ethoxypicolinic acidHCID 11846460—
ProductHCID 178467439HCID 178467439—

Reaction Steps

In a 20 mL vial a solution of Example 104A (32.5 mg, 0.16 mmol) dissolved in N,N-dimethylacetamide (0.8 mL) was added, followed by the addition of O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium tetrafluoroborate (50.4 mg, 0.16 mmol) dissolved in N,N-dimethylacetamide (0.8 mL). Then, c-(4-Methyl-1H-imidazol-2-yl)-methylamine hydrochloride (21.1 mg, 0.19 mmol) dissolved in N,N-dimethylacetamide (0.6 mL) was added followed by the addition of diisopropyl ethyl amine (57.9 uL, 0.31 mmol) dissolved in N,N-dimethylacetamide (0.8 mL). The mixture was shaken at room temperature overnight. The reaction was checked by LC/MS and concentrated to dryness. The residue was dissolved in 1:1 dimethyl sulfoxide/methanol and purified by reverse phase (0-70% CH3CN in 10 mM aq. ammonium acetate) to give the titled compound. 1H NMR (500 MHz, DMSO-d6) δ ppm 1.08-1.48 (m, 3H) 1.88-2.28 (m, 2H) 4.28-4.46 (m, 2H) 4.47-4.58 (m, 2H) 6.32-6.82 (m, 1H) 6.90-7.21 (m, 1H); MS (ESI) positive ion 301 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888374B2
Source datasetuspto-grants-2011_02
ORD IDord-f523cdd12f554d6cb78b108f63ee5ac3
Source noteuspto-grants-2011_02