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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191708Generated: November 1, 2026

6-Aminonicotinamide → HCID 86762306, compound

https://huagongshe.com/reaction/1191708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-AminonicotinamideHCID 9500—
ReactantHCID 16058694HCID 16058694—
ProductHCID 86762306HCID 86762306—

Reaction Steps

The product from Example 1, Part C (160 mg, 0.5 mmol) and 6-aminonicotinamide (103 mg, 0.75 mmol) were reacted as described in Example 5. After evaporation of the reaction solvent the residue was partitioned between water and EtOAc, and the aqueous phase was washed with EtOAc. The combined organics were washed with brine, dried (Na2SO4), filtered, and evaporated. The title compound was obtained by silica gel chromatography (10 mg, 5%). 1H NMR (300 MHz, CDCl3) δ 8.76 (d, J=2 Hz, 1H), 8.71 (br s, 1H), 8.22 (d, J=9 Hz, 1H), 8.13 (dd, J=9 Hz, 2 Hz, 1H), 7.20 (d, J=9 Hz, 2H), 6.83 (d, J=9 Hz, 2H), 5.05 (d, J=15 Hz, 1H), 4.63 (s, 1H), 4.13 (d, J=15 Hz, 1H), 3.77 (s, 3H), 2.94 (s, 2H), 1.95 (s, 3H), 1.83 (s, 3H). MS: m/z (MH+) 441.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680122B2
Source datasetuspto-grants-2014_03
ORD IDord-2ae3e4cf75804f0aa7f939363ffc2bae
Source noteuspto-grants-2014_03