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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875021Generated: October 31, 2026

Diisopropylethylamine → N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-5-({[(2-{[2-(methyloxy)ethyl]oxy}ethyl)oxy]acetyl}amino)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/1875021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(2-(2-Methoxyethoxy)ethoxy)acetic acidHCID 85241—
Reactant5-amino-N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-1H-indole-2-carboxamide trifluoroacetateHCID 86644884—
ReactantBOP chlorideHCID 131720136—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-5-({[(2-{[2-(methyloxy)ethyl]oxy}ethyl)oxy]acetyl}amino)-1H-indole-2-carboxamideHCID 5945158742%

Reaction Steps

BOP chloride (0.079 g, 0.309 mmol) was added to a solution of 5-amino-N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-1H-indole-2-carboxamide trifluoroacetate (0.060 g, 0.103 mmol), [(2-{[2-(methyloxy)ethyl]oxy}ethyl)oxy]acetic acid (0.016 mL, 0.103 mmol) and diisopropylethylamine (0.090 mL, 0.514 mmol) in DMF (1 mL). The mixture was stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate and water. The organic layer was washed with water, dried over sodium sulfate and concentrated. The residue was purified by reverse phase HPLC (acetonitrile:water with 0.1% trifluoroacetic acid) to give the title compound (0.027 g, 42%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 11.54 (s, 1H), 9.39 (s, 1H), 8.97 (t, 1H), 7.92 (s, 1H), 7.78 (s, 1H), 7.49 (d, 1H), 7.46 (s, 1H), 7.42-7.45 (m, 1H), 7.33-7.40 (m, 1H), 7.31 (s, 2H), 7.09 (d, 1H), 4.53 (d, 2H), 4.02 (s, 2H), 3.61-3.66 (m, 2H), 3.56-3.60 (m, 2H), 3.53 (dd, 2H), 3.38-3.44 (m, 2H), 3.19 (s, 3H). ES MS: m/z 629 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-1251b6307d7a4a32bfed2a79575ad550
Source noteuspto-grants-2012_11