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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875025Generated: November 4, 2026

Diisopropylethylamine → HCID 86644911, compound

https://huagongshe.com/reaction/1875025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Dimethylamino)propanoic acidHCID 239828—
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—
ProductHCID 86644911HCID 8664491134.1%

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), N,N-dimethyl-beta-alanine (0.016 g, 0.103 mmol) and diisopropylethylamine (0.11 mL, 0.617 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 triturated with methanol to give a white solid. Purification by reverse phase HPLC (acetonitrile:water with 0.1% TFA) gave the title compound (0.024 g, 34%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 11.56 (s, 1H), 10.04 (s, 1H), 9.17-9.45 (m, 1H), 8.96 (t, 1H), 7.92 (s, 1H), 7.78 (s, 1H), 7.42-7.50 (m, 2H), 7.29-7.40 (m, 2H), 7.23 (d, 1H), 7.08 (s, 1H), 4.53 (d, 2H), 3.31-3.39 (m, 2H), 2.71-2.82 (m, 8H). ES MS: m/z 568 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-3acc4321c5a645cd934211519336fa0c
Source noteuspto-grants-2012_11