HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191572Generated: November 2, 2026
Trifluoroacetic acid → HCID 54755744, compound
https://huagongshe.com/reaction/2191572
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 67002189 | HCID 67002189 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54755744 | HCID 54755744 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329699B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-d5ce5e260a8747dbaa4a8e6df6e84bce |
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| Source note | uspto-grants-2012_12 |
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