HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037796Generated: October 31, 2026
Triethylamine → 4-Acetyl-N-(2-oxo-2-((2,2,2-trifluoroethyl)amino)ethyl)-1-naphthalenecarboxamide
https://huagongshe.com/reaction/1037796
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-N-(2,2,2-trifluoroethyl)acetamide | HCID 24705143 | — |
| Reactant | 4-Acetyl-1-naphthalenecarbonyl chloride | HCID 86649801 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-Acetyl-N-(2-oxo-2-((2,2,2-trifluoroethyl)amino)ethyl)-1-naphthalenecarboxamide | HCID 66865191 | 75% |
Reaction Steps
A solution of 2-amino-N-(2,2,2-trifluoroethyl)acetamide (21.90 g, 0.14 mol) in 1,2-dichloroethane (80 mL) was added dropwise over 15 min to a solution of the product of Example 7, Step A (32.50 g, 0.14 mol) in 1,2-dichloroethane (160 mL) at a temperature of 25 to 30° C. The resulting mixture was further stirred for 10 min at 25° C. A solution of triethylamine (14.20 g, 0.14 mol) in 1,2-dichloroethane (80 mL) was then added dropwise over 44 min at 25° C., and the mixture was stirred further for 20 min at 25° C. The solvent was removed under reduced pressure, and the residue was dissolved in hot acetonitrile (50 mL). The mixture was then cooled to 25° C., and water (40 mL) was added dropwise. The mixture was further cooled to 0° C. and filtered. The isolated solid was washed with water (100 mL) and dried overnight in a vacuum oven (approximately 16-33 kPa at 50° C.) to provide the title product as an off-white solid (37 g, 75% yield) melting at 169-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546618B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-f1e41d41f8d643aea9a2e03aaa85f42a |
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| Source note | uspto-grants-2013_10 |
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