HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381907Generated: October 30, 2026
Diisopropylethylamine → HCID 25099513, compound
https://huagongshe.com/reaction/2381907
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate | HCID 42624899 | — |
| Reactant | 2-(3-Fluorophenyl)pyrimidine-5-carboxylic acid | HCID 45073363 | — |
| Reactant | HCID 68554957 | HCID 68554957 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 25099513 | HCID 25099513 | 60% |
Reaction Steps
A solution of 2-(3-fluoro-phenyl)-pyrimidine-5-carboxylic acid (372 mg, 1.7 mmol), HCTU (757 mg, 1.83 mmol), and DIPEA (780 μL, 4.47 mmol) in DMF (10 mL) is stirred at rt under N2 for 10 min. 5-Fluoro-3-methyl-indol-1-ylamine (250 mg, 1.52 mmol) is added. The resulting mixture is stirred at rt overnight. The mixture is 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 triturated in ether to afford 2-(3-fluoro-phenyl)-pyrimidine-5-carboxylic acid (5-fluoro-3-methyl-indol-1-yl)-amide (332 mg, 60%) as a solid. MS: 365 (M+H). 1H NMR (300 MHz, DMSO-d6): δ 12.08 (s, 1H), 9.43 (s, 2H), 8.36 (d, 1H), 8.20 (dt, 1H), 7.70-7.62 (m, 1H), 7.48 (dt, 1H), 7.40 (dd, 1H), 7.35 (dd, 1H), 7.32 (s, 1H), 7.03 (dt, 1H), 2.27 (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-afe95d7bb19545429703b3916deebc3b |
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| Source note | uspto-grants-2012_09 |
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