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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388393Generated: October 30, 2026

Diisopropylethylamine → HCID 44241540, compound

https://huagongshe.com/reaction/388393

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—
Reactant2-[3-(Ethyloxy)phenyl]-5-pyrimidinecarboxylic acidHCID 55113879—
Reactant(2-(Trifluoromethyl)-1h-indol-5-yl)methanamineHCID 58126817—
SolventDimethylformamideHCID 6228—
ProductHCID 44241540HCID 4424154045.4%

Reaction Steps

To a stirred solution of HATU (30.3 mg, 0.080 mmol) in DMF (1 ml) was added 2-[3-(ethyloxy)phenyl]-5-pyrimidinecarboxylic acid (Intermediate 7, 10 mg, 0.041 mmol) in DMF (0.5 ml), followed by DIPEA (0.021 ml, 0.120 mmol) and finally {[2-(trifluoromethyl)-1H-indol-5-yl]methyl}amine (Intermediate 4, 10 mg, 0.040 mmol) in DMF (1 ml). The solution was stirred for 24 hrs then DMF was removed using a rotary evaporator. DCM and sodium bicarbonate solution were then added to the residue. The mixture was poured through a phase separation cartridge, the organic layer evaporated to dryness and purified using MDAP to give the title compound as a yellow solid (8 mg);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377941B2
Source datasetuspto-grants-2013_02
ORD IDord-57df2fd63a79412fbae697c7abc68793
Source noteuspto-grants-2013_02