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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388391Generated: October 30, 2026

Diisopropylethylamine → 5-methoxy-N-[[2-(trifluoromethyl)-1H-indol-5-yl]methyl]pyrazine-2-carboxamide

https://huagongshe.com/reaction/388391

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—
Reactant5-Methoxy-2-pyrazinecarboxylic acidHCID 45789811—
Reactant(2-(Trifluoromethyl)-1h-indol-5-yl)methanamineHCID 58126817—
SolventDimethylformamideHCID 6228—
Product5-methoxy-N-[[2-(trifluoromethyl)-1H-indol-5-yl]methyl]pyrazine-2-carboxamideHCID 4446620160.7%

Reaction Steps

To a stirred solution of HATU (121 mg, 0.319 mmol) in DMF (1 ml) was added 5-(methyloxy)-2-pyrazinecarboxylic acid (AniChem LLC; 49.2 mg, 0.319 mmol) in DMF (0.5 ml), followed by DIPEA (0.084 ml, 0.479 mmol) and finally {[2-(trifluoromethyl)-1H-indol-5-yl]methyl}amine (Intermediate 4, 40 mg, 0.160 mmol) in DMF (1 ml). The solution was stirred for 24 hrs. DMF was removed using a rotary evaporator followed by addition of DCM and sodium bicarbonate solution. The mixture was poured through a phase separation cartridge. The organic layer was evaporated to dryness and purified using MDAP to give the title compound as a white solid (34 mg);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377941B2
Source datasetuspto-grants-2013_02
ORD IDord-1fbdf40e24c04bc5a0a45ec630b981ef
Source noteuspto-grants-2013_02