HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627035Generated: November 1, 2026
Trifluoroacetic acid → HCID 73603254, compound
https://huagongshe.com/reaction/627035
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131735258 | HCID 131735258 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 73603254 | HCID 73603254 | 67.2% |
Reaction Steps
For Example 10: To a solution of tert-butyl (S)-(2S)-1-((2S)-1-(2-(2-methoxyphenylcarbamoyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-1-yl)-3-methyl-1-oxobutan-2-ylamino)-1-oxopropan-2-yl(methyl)carbamate (40 mg, 72.2 μmol, Eq: 1.00) in DCM (2 mL) was added TFA (1 mL, 13.0 mmol, Eq: 180) and the resulting solution was stirred at rt. After 2 h, the reaction mixture was concentrated in vacuo, the residue was treated with saturated aqueous NaHCO3 (5 mL) and the resulting mixture was extracted with DCM (2×5 mL). The combined organic layers were concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 4 g, 0% to 10% MeOH in DCM) to give (S)-1-[(S)-3-methyl-2-((S)-2-methylamino-propionylamino)-butyryl]-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid (2-methoxyphenyl)-amide (22 mg), m/z=454 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309248B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-ade894197f534ae987267191a11bb5ac |
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| Source note | uspto-grants-2016_04 |
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