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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191699Generated: October 31, 2026

Triethylamine → HCID 58869944, compound

https://huagongshe.com/reaction/1191699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-AminopyridineHCID 10439—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 16058694HCID 16058694—
SolventAcetonitrileHCID 6342—
ProductHCID 58869944HCID 58869944—

Reaction Steps

The product from Example 1, Part C (200 mg, 0.6 mmol) was dissolved in 25 mL CH3CN, HOBt (48 mg, 0.3 mmol) was added, and stirring continued for 1 h. 2-Aminopyridine (88 mg, 0.9 mmol), triethylamine (0.18 mL, 1.26 mmol), and HATU (250 mg, 0.66 mmol) were added and the mixture was stirred at room temperature for 2 h. Solvent was evaporated and the title compound was isolated as a white solid by silica gel chromatography (140 mg, 56%). 1H NMR (400 MHz, CDCl3) δ 8.41 (br s, 1H), 8.29 (m, 1H), 8.13 (d, J=8 Hz, 1H), 7.70 (m, 1H), 7.22 (d, J=9 Hz, 2H), 7.06 (m, 1H), 6.83 (d, J=9 Hz, 2H), 5.07 (d, J=15 Hz, 1H), 4.62 (s, 1H), 4.15 (d, J=15 Hz, 1H), 3.77 (s, 3H), 2.90 (m, 2H), 1.95 (s, 3H), 1.84 (s, 3H). MS: m/z (MH+) 398.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680122B2
Source datasetuspto-grants-2014_03
ORD IDord-695caef5766b400cbbc7d16d68ff626e
Source noteuspto-grants-2014_03