HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360485Generated: October 31, 2026
Trifluoroacetic acid → HCID 58493941, compound
https://huagongshe.com/reaction/2360485
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 58493955 | HCID 58493955 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58493941 | HCID 58493941 | — |
Reaction Steps
220 mg tert-butyl (S)-3-{4-[2-(5-tert-butyl-3-methanesulphonylamino-2-methoxy-phenylcarbamoyl)-1-methyl-1H-indol-7-ylmethyl]-piperazine-1-carbonyl}-pyrrolidine-1-carboxylate are dissolved in 5 ml dichloromethane, combined with 231 μl trifluoroacetic acid and stirred for 12 hours at ambient temperature. Then the solvents are eliminated in vacuo, divided between saturated aqueous sodium hydrogen carbonate solution and dichloromethane and stirred vigorously for 30 minutes. The phases are separated, the aqueous phase is extracted twice with dichloromethane and the combined organic phases are dried on magnesium sulphate. Then the solvents are eliminated in vacuo and the crude product is chromatographed on silica gel (dichloromethane/(methanol-conc. ammonia 9:1) 90:10 to 80:20).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686022B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-0402ef4a768f4a16ac753f84fa6c7877 |
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| Source note | uspto-grants-2014_04 |
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