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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530448Generated: November 3, 2026

3,4-Diaminopyridine → HCID 178478056, compound

https://huagongshe.com/reaction/530448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DiaminopyridineHCID 5918—
Reactant6-Chloropicolinic acidHCID 20812—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
SolventDimethylformamideHCID 6228—
ProductHCID 178478056HCID 17847805637%

Reaction Conditions

Temperature120 °C

Reaction Steps

6-Chloropyridine-2-carboxylic acid (2.00 g, 12.7 mmol), 3,4-diaminopyridine (1.52 g, 14.0 mmol) and DIPEA (2.43 mL, 14.0 mmol) were dissolved in DMF (20 mL) and HBTU (5.29 g, 14.0 mmol) was added. The reaction mixture was stirred for 48 h and concentrated in vacuo. The residue was dissolved in EtOAc (100 mL), washed with 1 M aq Na2CO3 (2×100 mL), water (100 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography, dissolved in AcOH and heated at 120° C. for 50 min. The solvent was removed in vacuo and the residue was suspended in 1 M aq Na2CO3 (50 mL) and extracted with EtOAc (5×50 mL). The combined organic fractions were dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography and recrystallisation from MeOH to give the title compound (534 mg, 37%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353086B2
Source datasetuspto-grants-2016_05
ORD IDord-fc97a8d9b7b241b4a5825e5a4853868c
Source noteuspto-grants-2016_05