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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716069Generated: November 1, 2026

Trifluoroacetic acid → HCID 77981870, compound

https://huagongshe.com/reaction/716069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium Acetate TrihydrateHCID 23665404—
ReactantHCID 71015365HCID 71015365—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 77981870HCID 779818705.4%

Reaction Steps

To a 25 ml one necked round bottom flask, 3-(4-(7-pivaloyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)phenyl)-2-(1H-1,2,4-triazol-1-yl)acrylonitrile (0.052 g, 0.95 mmole) was taken in CH2Cl2 (5 mL). TFA (1.5 mL) was added drop wise at 0° C. After completion of the addition, the reaction mass was warmed up to RT and stirred for 16 hrs at the same temperature. After completion of the reaction, CH2Cl2 was distilled out to get solid. The solid was taken in ethanol (10 mL) and sodium acetate trihydrate (0.130 g, 0.95 mmole) was added at RT. The reaction mixture was stirred for 20 hrs at RT. After completion of the reaction the ethanol was distilled out under vacuum. To the residue, water (20 mL) was added and stirred for 15 min, filtered and wash with water and n-pentane. The solid was dried under vacuum to yield 21 mg of 3-(4-(7-pivaloyl-5H-pyrrolo[2,3-b]pyrazin-2-ylamino)phenyl)-2-(1H-1,2,4-triazol-1-yl)acrylonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187487B2
Source datasetuspto-grants-2015_11
ORD IDord-b95d16e187a74d9380a01f1c7eb8b602
Source noteuspto-grants-2015_11