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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239854Generated: November 2, 2026

Diisopropylethylamine → HCID 86648144, compound

https://huagongshe.com/reaction/239854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 68776901HCID 68776901—
ReactantHCID 86609688HCID 86609688—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86648144HCID 86648144—

Reaction Steps

(2S)-2-{[(1S)-1-(4-bromophenyl)-2,2,2-trifluoroethyl]amino}-4,4-dichlorobutanoic acid (120 mg) and (1S)-1-cyano-2-(4-cyano-2-fluorophenyl)ethanaminium chloride (66 mg) were dissolved in DMF (1.5 ml) and HATU (223 mg) was added. The reaction mixture was stirred at room temperature for 5 min and Hunig's base (204 μL) was added. The solution was stirred for 18 hours. The mixture was poured onto an aqueous sodium hydrogen carbonate (saturated, 20 ml) and water (20 ml). The mixture was stirred in an erlenmeyer flask for 10 min. The aqueous layer was extracted with EtOAc. The organic layer was washed with brine, dried on MgSO4. It was concentrated under reduced pressure. The crude product was purified by flash (eluted with 20:80 to 55:45 EtOAc/hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642799B2
Source datasetuspto-grants-2014_02
ORD IDord-3dc1282e13904d98b863efcd6ece4b32
Source noteuspto-grants-2014_02