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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898704Generated: October 27, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 6-Fluoro-pyridine-2-carboxylic Acid (6-chloro-5-propyl-pyrimidin-4-ylmethyl)-(3-methyl-butyl)-amide

https://huagongshe.com/reaction/898704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant6-Fluoropyridine-2-carboxylic acidHCID 226027—
Reactant(6-Chloro-5-propyl-pyrimidin-4-ylmethyl)-(3-methyl-butyl)-amineHCID 58661552—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product6-Fluoro-pyridine-2-carboxylic Acid (6-chloro-5-propyl-pyrimidin-4-ylmethyl)-(3-methyl-butyl)-amideHCID 58661550—

Reaction Steps

To a stirred solution of (6-chloro-5-propyl-pyrimidin-4-ylmethyl)-(3-methyl-butyl)-amine (0.715 g, 2.8 mmol) and 6-fluoro-pyridine-2-carboxylic acid (0.47 g, 3.34 mmol) in DCM (10 ml) is added EDCI (0.61 g) and DMAP (0.153 g). The mixture is stirred at room temperature overnight. DCM (10 ml) is added to dilute the mixture. The mixture is washed with water (5 mL), dried (Na2SO4) and solvent evaporated. Preparative TLC purification of the residue (2:1 of hexane: ethyl acetate) provides the title product. H1 NMR δ (CDCl3) 8.69 and 8.75 (s, 1H), 7.71-7.97 (m,1H), 7.58-60 (m, 1H), 4.79 and 5.07 (s, 2H), 3.50-3.64 (m, 21), 2.59-2.87 (m, 2H), 1.45-1.72 (m,5H), 0.92-1.09 (m, 4H), 0.81 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351826B2
Source datasetuspto-grants-2008_04
ORD IDord-1ac2e11b2a514b949b5fa48b073e2a7d
Source noteuspto-grants-2008_04