HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749481Generated: October 30, 2026
Trifluoroacetic acid → HCID 118162184, compound
https://huagongshe.com/reaction/1749481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131733590 | HCID 131733590 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118162184 | HCID 118162184 | 55% |
Reaction Steps
To a solution of tert-butyl ((1R,3S)-3-((2-((3-chlorophenethyl)amino)-5-cyanopyrimidin-4-yl)amino)-2,2-dimethylcyclobutyl)carbamate (82 mg, 0.17 mmol) in dry DCM (2 mL) was added trifluoroacetic acid (1.5 mL) dropwise under cooling in an ice-water bath. The resulting mixture was stirred at room temperature for 30 min. After removal of the organic solvent, the residue was neutralized with ammonia and extracted with DCM. The combined organic layers were dried over anhydrous sodium sulfate and concentrated to give the crude product, which was purified by standard methods to afford the title compound (34.3 mg, 0.092 mmol, 55% yield). 1H NMR (400 MHz, CD3OD) δ (ppm) 8.04 (s, 1H), 7.27-7.14 (m, 4H), 4.16-3.97 (m, 1H), 3.74-3.49 (m, 2H), 2.90-2.85 (m, 3H), 2.60-2.49 (m, 1H), 1.92-1.86 (m, 1H), 1.22 (s, 3H), 0.92 (s 3H). MS (ESI) m/z 371.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09156798B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-1e0c2135046449b58dc42722108870a0 |
|---|
| Source note | uspto-grants-2015_10 |
|---|