HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915592Generated: October 25, 2026
Lithium N-methylmethanaminide → 2-{[3-Tert-butyl-1-(2-methylphenyl)-1h-pyrazol-5-yl]amino}-4-(dimethylamino)benzoic acid
https://huagongshe.com/reaction/915592
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium N-methylmethanaminide | HCID 5152226 | — |
| Reactant | 2-{[3-Tert-butyl-1-(2-methylphenyl)-1h-pyrazol-5-yl]amino}-4-fluorobenzoic acid | HCID 58958582 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-{[3-Tert-butyl-1-(2-methylphenyl)-1h-pyrazol-5-yl]amino}-4-(dimethylamino)benzoic acid | HCID 58958609 | 15% |
Reaction Steps
To a solution of 2-{[3-tert-butyl-1-(2-methylphenyl)-1H-pyrazol-5-yl]amino}-4-fluorobenzoic acid (Example 248, 35 mg, 0.09 mmol) in THF (1 mL) at −40° C. was added LiNMe2 (0.19 mL, 1 M in hexanes) under nitrogen. The mixture was then stirred at this temperature for 30 min, and then gradually warmed to rt over a 4 h period. The pH of the solution was adjusted to pH 5, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The crude was purified by HPLC using gradient elution from 10 to 80% acetonitrile in water to afford 5.7 mg (15%) of the title compound. 1H NMR (300 MHz, CD2Cl2) δ 9.55 (s, 1H), 7.73 (d, 1H), 7.22-7.35 (m, 4H), 6.44 (d, 1H), 6.18 (dd, 1H), 6.15 (s, 1H), 3.00 (s, 6H), 2.04 (s, 3H), 1.32 (s, 9H). ES-MS m/z 393.2 (MH30 ); HPLC RT (min) 2.84.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07265144B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-8c2db87082454790adc8c54f20ad1b7c |
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| Source note | uspto-grants-2007_09 |
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