HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469814Generated: October 31, 2026
Dimethylformamide → 2-Chloro-5-(pivalamidomethyl)-N-(8-((3-(trifluoromethyl)phenyl)amino)quinolin-4-yl)benzamide
https://huagongshe.com/reaction/1469814
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Nitrophenyl 2-chloro-5-(pivalamidomethyl)benzoate | HCID 86692238 | — |
| Reactant | N-(3-(trifluoromethyl)phenyl)quinoline-4,8-diamine | HCID 86692281 | — |
| Product | 2-Chloro-5-(pivalamidomethyl)-N-(8-((3-(trifluoromethyl)phenyl)amino)quinolin-4-yl)benzamide | HCID 86692280 | — |
Reaction Steps
To a solution of N-(3-(trifluoromethyl)phenyl)quinoline-4,8-diamine (Intermediate-12, 80 mg, 0.264 mmol) in DMF (2 mL) was added NaH (26 mg, 0.65 mmol, 60% in mineral oil) at 0° C. and the reaction mixture was stirred at 0-5° C. for 30 minutes. Then a solution of 4-nitrophenyl 2-chloro-5-(pivalamidomethyl)benzoate (Intermediate-13, 123 mg, 0.314 mmol) in DMF (1 mL) was added to the reaction mixture at 0° C. and the reaction mixture was stirred at 0° C.—rt for 2 h. Then the reaction mixture was quenched with water and was extracted with EtOAc. The organic layer was washed with brine, separated, dried, filtered and concentrated. The residue was purified by column chromatography to afford 15 mg of the title product. 1H NMR (300 MHz, DMSO-d6): δ 10.92 (s, 1H), 9.07 (s, 1H), 8.86 (d, J=4.8 Hz, 1H), 8.21-8.18 (m, 2H), 7.80-7.57 (m, 3H), 7.59-7.54 (m, 5H), 7.39 (d, J=8.4 Hz, 1H), 7.25 (d, J=7.2 Hz, 1H), 4.32 (d, J=6.0 Hz, 2H), 1.19 (s, 9H); MS [M+H]+: 555.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006257B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-6bafbb161c4f4c8f91ccf29b45c45746 |
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| Source note | uspto-grants-2015_04 |
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