Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908980Generated: October 28, 2026

2-Amino-4-methylthiazole → 4-(methyl(pyridin-3-yl)amino)-N-(4-methylthiazol-2-yl)picolinamide

https://huagongshe.com/reaction/1908980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methylthiazoleHCID 74143—
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 58349312HCID 58349312—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-(methyl(pyridin-3-yl)amino)-N-(4-methylthiazol-2-yl)picolinamideHCID 8676217326.9%

Reaction Steps

Compound 12 (0.1 g, 0.4 mmol, 1 eq), 4-methylthiazol-2-amine (60 mg, 0.53 mmol, 1.2 eq), 2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (348 mg, 0.915 mmol, 2.10 eq), and DIEA (160 μL, 0.915 mmol, 2.10 eq) were dissolved in CH2Cl2 (5 mL) and DMF (1 mL) and stirred rt for 48 h. The reaction was diluted with CH2Cl2 and washed with water (1×). The organics were dried (MgSO4), filtered and concentrated in vacuo. Purification by flash chromatography on silica gel afforded 35 mg (25%) of the title compound as a white solid: 1H NMR (400 MHz, CDCl3) δ 8.60 (d, J=2.3 Hz, 1H), 8.56 (dd, J=4.7, 1.1 Hz, 1H), 8.33 (d, J=4.8 Hz, 1H), 7.83 (ddd, J=8.2, 2.4, 1.5 Hz, 1H), 7.55 (dd, J=8.1, 4.7 Hz, 1H), 7.31 (s, 1H), 6.94-6.89 (m, 1H), 8.86 (s, 1H), 3.40 (s, 3H), 2.28 (s, 3H); [M+1]+: 326.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598345B2
Source datasetuspto-grants-2013_12
ORD IDord-e5a1a21d7ad346c799ff4af692ed3456
Source noteuspto-grants-2013_12