HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671763Generated: October 31, 2026
2-(Trifluoromethyl)benzylamine → HCID 178482417, compound
https://huagongshe.com/reaction/1671763
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Trifluoromethyl)benzylamine | HCID 76447 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 178482422 | HCID 178482422 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178482417 | HCID 178482417 | 71% |
Reaction Steps
A solution of cis-4-(4-(methylamino)-6-(piperidin-1-yl)-1,3,5-triazin-2-ylamino)cyclohexanecarboxylic acid (7.6 mg, 0.023 mmol, 1 equivalent), 2-trifluoromethyl benzylamine (4 μL, 0.03 mmol, 1.25 equivalents) and DMAP (0.6 mg, 0.2 equivalents) in dichloromethane (1.5 ml) was cooled with stirring in an ice bath. EDCl (6.6 mg, 0.034 mmol, 1.5 equivalents) was added. The reaction mixture was stirred at 0° C. for 30 min and at room temperature for 2-3 hours. The solution was diluted with dichloromethane (1 ml), which was further washed with saturated sodium bicarbonate and water. The organic layer was dried and purified by HPLC (Luna 5μ C8(2), 100×21 mm, 28-70% CH3CN/H2O, 0.1% TFA, 20 min) to afford the final product (8.0 mg, yield 71%). MS (ES+): m/e 492.30 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994317B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-8f3c96cd591040ac9bf37d269a3585e0 |
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| Source note | uspto-grants-2011_08 |
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