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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898544Generated: October 29, 2026

Trifluoroacetic acid → HCID 53385937, compound

https://huagongshe.com/reaction/1898544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67386157HCID 67386157—
SolventDichloromethaneHCID 6344—
ProductHCID 53385937HCID 5338593746%

Reaction Steps

To a solution of 2-phenoxy-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [(R)-2-methyl-1-(pyrrolidine-1-carbonyl)-propyl]-amide from Step 3 in dichloromethane (0.5 mL) was added trifluoroacetic acid (0.7 mL). The reaction mixture was stirred at room temperature overnight then concentrated. The residue was stirred with THF (1 mL), water (0.5 mL), and Et3N (0.5 mL) for 2 h then concentrated. The residue was partitioned between ethyl acetate and water and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over MgSO4 and concentrated. The residue was purified by SiO2 column chromatography (5% MeOH/CH2Cl2) to provide 0.049 g (46%, 2 steps) of 2-phenoxy-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid [(R)-2-methyl-1-(pyrrolidine-1-carbonyl)-propyl]-amide as a white foam. MS: 408 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518945B2
Source datasetuspto-grants-2013_08
ORD IDord-f21d81cfe7b34f218862f9a192dc3b0c
Source noteuspto-grants-2013_08