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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177352Generated: October 30, 2026

2-Amino-5-methylpyridine → HCID 59559959, compound

https://huagongshe.com/reaction/1177352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methylpyridineHCID 15348—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 59559998HCID 59559998—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59559959HCID 5955995927%

Reaction Steps

HATU (431 mg, 1.13 mmol) was added to a mixture of 6-methoxy-2-methyl-1H-benzoimidazole-4-carboxylic acid (350 mg, 1.0 mmol), 2-amino-5-picoline (134 mg, 1.24 mmol), and DIEA (0.359 mL, 2.06 mmol) in DMF (5 mL) while stirring at room temperature. The resulting mixture was stirred at room temperature under N2 atmosphere for 16 hours. The mixture was worked up with water and extracted into chloroform; the organic layer was dried over MgSO4, concentrated. The crude product was purified by flash silicagel chromatography (ISCO) eluting with CHCl3:MeOH (95:5) to gain 85 mg light brown color solid product in 27% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 12.68 (s, 1 H) 12.41 (s, 1 H) 8.27 (d, J=8.56 Hz, 1 H) 8.23 (s, 1 H) 7.68 (dd, J=8.56, 1.76 Hz, 1 H) 7.51 (d, J=2.27 Hz, 1 H) 7.23 (d, J=2.27 Hz, 1 H) 3.85 (s, 3 H) 2.61 (s, 3 H) 2.29 (s, 3 H). LRMS for C16H16N4O2 m/z 297 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-33ace2a7508f46d081b3912395bf7952
Source noteuspto-grants-2010_11