HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381920Generated: October 29, 2026
Diisopropylethylamine → HCID 25099555, compound
https://huagongshe.com/reaction/2381920
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10584602 | HCID 10584602 | — |
| Reactant | ((7-Azabenzotriazol-1-YL)oxy)tris(pyrrolidino)phosphonium hexafluorophosphate | HCID 11038641 | — |
| Reactant | 2-(3-Fluorophenyl)-4-methylpyrimidine-5-carboxylic acid | HCID 61702587 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 25099555 | HCID 25099555 | 24.4% |
Reaction Steps
A solution of 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (596 mg, 2.57 mmol), PyAOP (2.63 mmol), and DIPEA (830 μL, 4.75 mmol) in DCM (20 mL) is stirred at rt under N2 for 10 min. 5-Bromoindol-1-ylamine (500 mg, 2.37 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 purified by silica gel chromatography eluting with 2% MeOH in DCM to afford 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (5-bromo-indol-1-yl)-amide (246 mg, 24%) as a solid. MS: 425 (M) & 427 (M+2). 1H NMR (300 MHz, DMSO-d6): δ 12.02 (s, 1H), 9.24 (s, 1H), 8.34 (d, 1H), 8.20-8.15 (m, 1H), 7.84 (d, 1H), 7.68-7.61 (m, 1H), 7.59 (d, 1H), 7.50-7.43 (m, 2H), 7.35 (dd, 1H), 6.57 (dd, 1H), 2.78 (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-e8ca09b0e2654ee1b83793de40624ed4 |
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| Source note | uspto-grants-2012_09 |
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