HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874951Generated: November 4, 2026
Diisopropylethylamine → HCID 59451493, compound
https://huagongshe.com/reaction/1874951
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 3-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile | HCID 59451392 | — |
| Reactant | HCID 68480831 | HCID 68480831 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59451493 | HCID 59451493 | 50% |
Reaction Steps
HATU (0.061 g, 0.161 mmol) was added as a solid to a DMF (1 mL) solution of 3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.050 g, 0.161 mmol), 5-{[3-(methylthio)propyl]oxy}-1H-indole-2-carboxylic acid (0.043 g, 0.161 mmol) and DIPEA (0.028 mL, 0.161 mmol). After stirring for 2 hours the reaction mixture was poured into EtOAc and water and the layers separated. The organic layer was dried over MgSO4, filtered and the solvent evaporated. The residue was dissolved in MeOH and purification was accomplished by reverse-phase HPLC (water/acetonitrile with 0.1% TFA) to afford the title compound (0.045 g, 50%) as a light yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 11.45 (s, 1H), 8.96 (t, 1H), 7.80 (s, 1H), 7.43-7.54 (m, 3H), 7.37 (t, 1H), 7.28 (d, 1H), 7.01-7.10 (m, 2H), 6.82 (dd, 1H), 4.54 (d, 2H), 4.00 (t, 2H), 2.61 (t, 2H), 2.04 (s, 3H), 1.89-2.01 (m, 2H). LCMS: m/z 558.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-58e8a64f0e4f4709a1ddb1dca2dfefe6 |
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| Source note | uspto-grants-2012_11 |
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