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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874834Generated: November 2, 2026

Diisopropylethylamine → 1,1-dimethylethyl (2-{[({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)amino]carbonyl}-1H-indol-6-yl)carbamate

https://huagongshe.com/reaction/1874834

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—
Reactant6-(Tert-butoxycarbonylamino)-1h-indole-2-carboxylic acidHCID 59451539—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1,1-dimethylethyl (2-{[({4-chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)amino]carbonyl}-1H-indol-6-yl)carbamateHCID 5945152354%

Reaction Steps

HATU (0.104 g, 0.272 mmol) was added to a solution of 3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.056 g, 0.182 mmol), 6-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-1H-indole-2-carboxylic acid (0.050 g, 0.182 mmol) and DIPEA (0.048 mL, 0.272 mmol) in DMF (1.5 mL). The mixture was stirred at RT for 1.5 h. The reaction mixture was diluted with ethyl acetate and water. The organic layer was washed with water and brine, dried over sodium sulfate, and the solvent was evaporated. The residue was purified by column chromatography (hexane/EtOAc) to give the title compound (0.056 g, 48%) as an off-white solid. 1H NMR (400 MHz, CDCl3): δ ppm 9.74 (s, 1H), 7.78 (s, 1H), 7.44 (d, 1H), 7.27-7.37 (m, 2H), 7.21 (dd, 1H), 7.08-7.13 (m, 1H), 6.98 (d, 1H), 6.74-6.86 (m, 3H), 6.63 (s, 1H), 4.66 (d, 2H), 1.50 (s, 9H). MS: m/z 569 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-25cf22fe2140497894943debe9721b30
Source noteuspto-grants-2012_11