HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381918Generated: October 31, 2026
Diisopropylethylamine → HCID 25099553, compound
https://huagongshe.com/reaction/2381918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (Dimethylamino)-N,N-dimethyl((1-oxo-1lambda~5~-pyridin-2-yl)sulfanyl)methaniminium hexafluorophosphate | HCID 10571248 | — |
| Reactant | 2-(3-Fluorophenyl)-4-methylpyrimidine-5-carboxylic acid | HCID 61702587 | — |
| Reactant | HCID 68554528 | HCID 68554528 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 25099553 | HCID 25099553 | 49% |
Reaction Steps
A solution of 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (764 mg, 3.29 mmol), HOTT (1.33 g, 3.58 mmol), and DIPEA (1.65 mL, 9.45 mmol) in DMF (15 mL) is stirred at rt under N2 for 10 min. 2,3-Dimethyl-indol-1-ylamine (497 mg, 3.1 mmol) is added. The resulting mixture is stirred at 80° C. overnight. The mixture is cooled and portioned between EtOAc and water. The organic phase is separated, washed with saturated aqueous NaHCO3, water and brine, dried (MgSO4), filtered and concentrated in vacuo. The residue is purified by silica gel chromatography eluting with 20% EtOAc in heptane to afford 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (2,3-dimethyl-indol-1-yl)-amide (568 mg, 49%) as a solid. MS: 375 (M+H). 1H NMR (300 MHz, DMSO-d6): δ 11.68 (s, 1H), 9.24 (s, 1H), 8.33 (d, 1H), 8.20-8.15 (m, 1H), 7.69-7.61 (m, 1H), 7.50-7.43 (m, 2H), 7.37 (d, 1H), 7.17-7.05 (m, 2H), 2.78 (s, 3H), 2.30 (s, 3H), 2.24 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258130B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-891ed0e6d6764518945510a7c500435b |
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| Source note | uspto-grants-2012_09 |
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