HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222957Generated: October 31, 2026
Trifluoroacetic acid → HCID 11599367, compound
https://huagongshe.com/reaction/2222957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 86604044 | HCID 86604044 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11599367 | HCID 11599367 | 55.8% |
Reaction Steps
To a cold solution of 3-[(S)-2-[4-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-2,5-dioxo-imidazolidin-1-yl]-2-(4-methoxycarbonyl-thiazol-2-ylcarbamoyl)-ethyl]-indole-1-carboxylic acid tert-butyl ester (78 mg, 0.118 mmol) in dichloromethane (10 mL), was added trifluoroacetic acid (2 mL, 26.0 mmol). The reaction mixture was stirred at room temperature for 1 hour. The volatiles were removed in vacuo and the residue was dissolved in ethyl acetate (100 mL), washed once with cold saturated aqeous sodium bicarbonate, water, brine and dried over sodium sulfate. The solvent was removed and the residue was purified by chromatographed over silica gel gradient eluted between 50% and 75% ethyl acetate in hexanes to afford 2-[(S)-2-[4-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-2,5-dioxo-imidazolidin-1-yl]-3-(1H-indol-3-yl)-propionylamino]-thiazole-4-carboxylic acid methyl ester (37 mg, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07371869B2 |
|---|
| Source dataset | uspto-grants-2008_05 |
|---|
| ORD ID | ord-c5d2ee4b569e439c8b5a2411f8d5c587 |
|---|
| Source note | uspto-grants-2008_05 |
|---|