HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406248Generated: October 31, 2026
Trifluoroacetic acid → HCID 67980541, compound
https://huagongshe.com/reaction/2406248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 86667200 | HCID 86667200 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67980541 | HCID 67980541 | 59.3% |
Reaction Steps
To a solution of 2-methyl-4-{3-[4-((R)-3-morpholin-4-yl-1-phenylsulfonylmethylpropyl-amino)-3-trifluoromethanesulfonyl-benzenesulfonylamino]-5,6-dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazin-7-yl}-piperidine-1-carboxylic acid tert-butyl ester (42 mg, 0.048 mmol) in CH2Cl2 (1 mL) under nitrogen was added trifluoroacetic acid (0.093 mL, 1.203 mmol) and the reaction was stirred for 2.5 hours. The reaction mixture was then concentrated and diluted with water and CH2Cl2. It was then basified to pH approximately 8 with saturated Na2CO3. The aqueous layer was extracted three times with CH2Cl2. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to afford N-[7-(2-methyl-piperidin-4-yl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazin-3-yl]-4-((R)-3-morpholin-4-yl-1-phenylsulfanylmethyl-propylamino)-3-trifluoromethanesulfonyl-benzenesulfonamide (22 mg, 59% yield). MS [m/z; (M+1)+]: 773.6
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809352B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-d52a271c84234cb68bcc780aecde726e |
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| Source note | uspto-grants-2014_08 |
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