HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406224Generated: November 1, 2026
Trifluoroacetic acid → HCID 178527558, compound
https://huagongshe.com/reaction/2406224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 67980827 | HCID 67980827 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178527558 | HCID 178527558 | 99% |
Reaction Steps
To a solution of 3-[4-((R)-3-morpholin-4-yl-1-phenylsulfanylmethyl-propylamino)-3-trifluoromethanesulfonyl-benzenesulfonylamino]-5,6-dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazine-7-carboxylic acid tert-butyl ester (130 mg, 0.168 mmol) in dichloromethane (3 mL) under nitrogen was added trifluoroacetic acid (0.323 mL, 4.19 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 organics were extracted three times with CH2Cl2. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to afford the title compound (112 mg, 99% yield). MS [m/z; (M+1)+]: 676.5
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-6b32324ff4cf491f99b345b39ca784e8 |
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| Source note | uspto-grants-2014_08 |
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