Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875022Generated: November 3, 2026

Diisopropylethylamine → HCID 68485564, compound

https://huagongshe.com/reaction/1875022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
Reactant5-amino-N-({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-1H-indole-2-carboxamide trifluoroacetateHCID 86644884—
ReactantBOP chlorideHCID 131720136—
SolventDimethylformamideHCID 6228—
ProductHCID 68485564HCID 6848556441.4%

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), 1-{[(1,1-dimethylethyl)oxy]carbonyl}-4-piperidinecarboxylic acid (0.0236 g, 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 extracted with ethyl acetate and water. The organic layer was washed with water, dried over sodium sulfate and concentrated. The residue was purified by flash chromatography with hexane:ethyl acetate to give the title compound (0.029 g, 41%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 11.50 (br. s., 1H), 9.72 (br. s., 1H), 8.95 (br. s., 1H), 7.95 (s, 1H), 7.78 (s, 1H), 7.41-7.52 (m, 2H), 7.36 (t, 1H), 7.25-7.32 (m, 1H), 7.21 (d, 1H), 7.06 (br. s., 1H), 4.52 (d, 2H), 3.85-4.17 (m, 2H), 2.58-2.94 (m, 2 H), 1.63-1.85 (m, 2H), 1.41-1.53 (m, 2H), 1.36 (s, 9H). ES MS: m/z 680 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-3ce58cae1e89467c8328071a8527ec6d
Source noteuspto-grants-2012_11