Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381907Generated: October 30, 2026

Diisopropylethylamine → HCID 25099513, compound

https://huagongshe.com/reaction/2381907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphateHCID 42624899—
Reactant2-(3-Fluorophenyl)pyrimidine-5-carboxylic acidHCID 45073363—
ReactantHCID 68554957HCID 68554957—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 25099513HCID 2509951360%

Reaction Steps

A solution of 2-(3-fluoro-phenyl)-pyrimidine-5-carboxylic acid (372 mg, 1.7 mmol), HCTU (757 mg, 1.83 mmol), and DIPEA (780 μL, 4.47 mmol) in DMF (10 mL) is stirred at rt under N2 for 10 min. 5-Fluoro-3-methyl-indol-1-ylamine (250 mg, 1.52 mmol) is added. The resulting mixture is stirred at rt overnight. The mixture is portioned between EtOAc and water. The organic phase is separated, washed with saturated aqueous NaHCO3, water and brine, dried (MgSO4), filtered and concentrated in vacuo. The residue is triturated in ether to afford 2-(3-fluoro-phenyl)-pyrimidine-5-carboxylic acid (5-fluoro-3-methyl-indol-1-yl)-amide (332 mg, 60%) as a solid. MS: 365 (M+H). 1H NMR (300 MHz, DMSO-d6): δ 12.08 (s, 1H), 9.43 (s, 2H), 8.36 (d, 1H), 8.20 (dt, 1H), 7.70-7.62 (m, 1H), 7.48 (dt, 1H), 7.40 (dd, 1H), 7.35 (dd, 1H), 7.32 (s, 1H), 7.03 (dt, 1H), 2.27 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-afe95d7bb19545429703b3916deebc3b
Source noteuspto-grants-2012_09