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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381947Generated: October 31, 2026

Dimethylformamide → HCID 25099693, compound

https://huagongshe.com/reaction/2381947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(3-Fluorophenyl)-4-methylpyrimidine-5-carboxylic acidHCID 61702587—
ReactantHCID 68555047HCID 68555047—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventSodium CarbonateHCID 10340—
ProductHCID 25099693HCID 2509969370%

Reaction Steps

A solution of 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (250 mg, 1.07 mmol) in DCM (10 mL) is cooled to 0° C., treated with DMF (20 μL) and ClCOCOCl (280 μL, 3.21 mmol), and stirred for 20 min. Toluene (10 mL) is added and the mixture is concentrated in vacuo. The residue is dissolved in pyridine (10 mL) and treated with DMAP (5 mg) and 1-(1-amino-5-fluoroindol-3-yl)-2-methyl-propan-2-ol (0.72 mmol). The mixture is stirred at rt for 12 h. The mixture is diluted with saturated aqueous Na2CO3, extracted with EtOAc. The organic layer is separated, dried (Na2SO4), filtered and concentrated in vacuo. The residue is purified by silica gel chromatography eluting with 20%-60% EtOAc in heptane to afford 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid [5-fluoro-3-(2-hydroxy-2-methyl-propyl)-indol-1-yl]-amide (218 mg, 70%). MS: 437 (M+H); 1H NMR (300 MHz, DMSO-d6): δ 1.14 (s, 6H), 2.77 (s, 2H), 3.29 (s, 3H), 7.03 (m, 1H), 7.37 (s, 1H), 7.35-7.55 (m, 3H), 7.65 (m, 1H), 8.19 (m, 1H), 8.34 (m, 1H), 9.22 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-c16c7fd827914b309b56215594b40595
Source noteuspto-grants-2012_09