HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972770Generated: November 2, 2026
Potassium Carbonate → 5-(2-benzyl-2H-indazol-6-yl)-7-[4-(4-propylpiperazin-1-yl)phenyl]pyrrolo[2,1-f][1,2,4]triazin-4-amine
https://huagongshe.com/reaction/1972770
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | 5-(2-benzyl-2H-indazol-6-yl)-7-(4-piperazin-1-ylphenyl)pyrrolo[2,1-f][1,2,4]triazin-4-amine | HCID 58529498 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(2-benzyl-2H-indazol-6-yl)-7-[4-(4-propylpiperazin-1-yl)phenyl]pyrrolo[2,1-f][1,2,4]triazin-4-amine | HCID 58529422 | 25.8% |
Reaction Steps
To a solution of 5-(2-benzyl-2H-indazol-6-yl)-7-(4-piperazin-1-ylphenyl)pyrrolo[2,1-f][1,2,4]triazin-4-amine (75 mg, 0.15 mmol) and 1-iodopropane (31 mg, 0.18 mmol) in DMF (2 mL) was added potassium carbonate (37 mg, 0.27 mmol). The reaction was heated (50° C.) for 17 h. The reaction was cooled to rt and was partitioned between ethyl acetate (25 mL) and H2O (25 mL). The layers were separated and the organic was washed with brine, dried (Na2SO4) and concentrated. The residue was purified by preparative HPLC using a gradient elution from 15% to 50% acetonitrile in water followed by trituration with Et2O to obtain 21 mg (25%) of the desired product. 1H NMR (300 MHz, DMSO-d6) δ 8.55 (s, 1 H), 7.97-7.91 (m, 3 H), 7.81 (d, 1 H), 7.65 (s, 1 H), 7.37-7.26 (m, 5H), 7.19 (d, 1 H), 7.04-6.96 (m, 3 H), 5.66 (s, 2 H), 325-3.15 (m, 4 H), 2.51-2.48 (m, 4 H), 2.32-2.24 (m, 2 H), 1.53-1.42 (m, 2 H), 0.88 (t, 3 H), 2.89 (s, 4 H); ES-MS m/z 543.4 [M+H]+, HPLC RT (min) 2.40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431695B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-bdad6782e96f4c138abe9d13c0fd613b |
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| Source note | uspto-grants-2013_04 |
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