HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485906Generated: October 31, 2026
Trifluoroacetic acid → HCID 73295229, compound
https://huagongshe.com/reaction/1485906
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131736769 | HCID 131736769 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 73295229 | HCID 73295229 | — |
Reaction Steps
To a solution of tert-butyl (S)-1-((S)-1-((S)-3-(2,6-difluorophenylcarbamoyl)-3,4-dihydro isoquinolin-2 (1H)-yl)-3-methyl-1-oxobutan-2-ylamino)-1-oxopropan-2-yl(methyl)carbamate (138 mg, 241 μmol, Eq: 1.00) in DCM (2 mL) was added TFA (2.96 g, 2 mL, 26.0 mmol, Eq: 108) and the resulting solution stirred at RT for 1 h. The mixture was concentrated in vacuo, saturated NaHCO3 was added to the residue and the resulting mixture extracted with DCM. The combined extracts were dried over Na2SO4 and concentrated in vacuo. The residue was treated with ether/hexanes to give (S)-2-[(S)-3-methyl-2-((S)-2-methylamino-propionylamino)-butyryl]-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid (2,6-difluoro-phenyl)-amide as a white solid which was used without purification (70 mg), m/z=473 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422332B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-8f88afc6416c44158d09989e60f8733c |
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| Source note | uspto-grants-2016_08 |
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