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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191572Generated: November 2, 2026

Trifluoroacetic acid → HCID 54755744, compound

https://huagongshe.com/reaction/2191572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67002189HCID 67002189—
SolventDichloromethaneHCID 6344—
ProductHCID 54755744HCID 5475574481%

Reaction Steps

In a 10 mL round-bottomed flask, 2-cyclopropyl-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-methanesulfonyl-piperidin-3-yl)-amide (173 mg, 0.35 mmol) was dissolved in CH2Cl2 (1.4 mL). Trifluoroacetic acid (1.1 mL) was added and the light yellow reaction mixture was stirred at room temperature for 2 h then concentrated. The residue was taken up in toluene (3 mL), concentrated and then dried under high vacuum. The residue was dissolved in CH2Cl2 (1.4 mL) and ethylenediamine (1.4 mL) was added. The reaction mixture was stirred at room temperature for 2 h then H2O and EtOAc were added. The resultant suspension was filtered, rinsing with H2O and EtOAc and dried under high vacuum to afford 103 mg (81%) of 2-cyclopropyl-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (1-methanesulfonyl-piperidin-3-yl)-amide as an off-white solid. MS: (M+H)+=364; mp=284.0-287.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329699B2
Source datasetuspto-grants-2012_12
ORD IDord-d5ce5e260a8747dbaa4a8e6df6e84bce
Source noteuspto-grants-2012_12