Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874951Generated: November 4, 2026

Diisopropylethylamine → HCID 59451493, compound

https://huagongshe.com/reaction/1874951

Reaction equation

Participants

RoleNameHCIDCharge
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—
Reactant3-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrileHCID 59451392—
ReactantHCID 68480831HCID 68480831—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59451493HCID 5945149350%

Reaction Steps

HATU (0.061 g, 0.161 mmol) was added as a solid to a DMF (1 mL) solution of 3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.050 g, 0.161 mmol), 5-{[3-(methylthio)propyl]oxy}-1H-indole-2-carboxylic acid (0.043 g, 0.161 mmol) and DIPEA (0.028 mL, 0.161 mmol). After stirring for 2 hours the reaction mixture was poured into EtOAc and water and the layers separated. The organic layer was dried over MgSO4, filtered and the solvent evaporated. The residue was dissolved in MeOH and purification was accomplished by reverse-phase HPLC (water/acetonitrile with 0.1% TFA) to afford the title compound (0.045 g, 50%) as a light yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 11.45 (s, 1H), 8.96 (t, 1H), 7.80 (s, 1H), 7.43-7.54 (m, 3H), 7.37 (t, 1H), 7.28 (d, 1H), 7.01-7.10 (m, 2H), 6.82 (dd, 1H), 4.54 (d, 2H), 4.00 (t, 2H), 2.61 (t, 2H), 2.04 (s, 3H), 1.89-2.01 (m, 2H). LCMS: m/z 558.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-58e8a64f0e4f4709a1ddb1dca2dfefe6
Source noteuspto-grants-2012_11