HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524098Generated: October 30, 2026
Trifluoroacetic acid → HCID 86713612, compound
https://huagongshe.com/reaction/524098
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Propanesulfonyl chloride | HCID 66279 | — |
| Reactant | HCID 86713613 | HCID 86713613 | — |
| Reactant | HCID 86713614 | HCID 86713614 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86713612 | HCID 86713612 | 25.2% |
Reaction Steps
To a solution tert-butyl(1-(2-((2-nitrophenyl)amino)pyrimidin-4-yl)piperidin-3-yl)carbamate (0.14 g, 0.34 mmol) in DCM (2.0 mL) was added TFA (1.0 mL) and the mixture was stirred for 1 h. An aliquot of the reaction mixture was analyzed by LCMS, which indicated that the reaction had proceeded to completion. The solvents were removed and the residue was dried on high vacuum. The crude product was used for the next step without further purification. To a solution of 4-(3-aminopiperidin-1-yl)-N-(2-nitrophenyl)pyrimidin-2-amine (0.34 mmol) in DCM (3.5 mL) at 0° C. was added propane-1-sulfonyl chloride (0.045 mL, 0.4 mmol) and triethylamine (0.12 mL, 0.85 mmol) and the mixture was warmed to room temperature overnight. The crude reaction mixture was concentrated and purified by flash chromatography (0-7.5% MeOH/DCM) to give the title compound (36 mg, 24% yield). MS (ES+) C18H24N6O4S requires: 420. found: 421 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340514B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-184b249db964489d9cdaf61a6d2dc486 |
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| Source note | uspto-grants-2016_05 |
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