HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695041Generated: October 31, 2026
Dimethylformamide → n-(2-Amino-4-fluorophenyl)-6-(2-(2-(((5-fluoro-2-oxoindolin-3-ylidene)-hydrazono)methyl)-3,5-dimethyl-1h-pyrrole-4-carboxamido)ethylamino)nicotinamide
https://huagongshe.com/reaction/1695041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | N-(2-amino-4-fluorophenyl)-6-(2-aminoethylamino)nicotinamide | HCID 57993718 | — |
| Reactant | 2-(((5-Fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-4-carboxylic acid | HCID 137252512 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | n-(2-Amino-4-fluorophenyl)-6-(2-(2-(((5-fluoro-2-oxoindolin-3-ylidene)-hydrazono)methyl)-3,5-dimethyl-1h-pyrrole-4-carboxamido)ethylamino)nicotinamide | HCID 136656692 | 68% |
Reaction Steps
2-(((5-Fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-4-carboxylic acid (328 mg, 1 mmol) and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (384 mg, 2 mmol), hydroxybenzotriazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and N-(2-amino-4-fluorophenyl)-6-(2-aminoethylamino)nicotinamide (303 mg, 1.05 mmol) were added. The mixture was stirred for 20 hours at room temperature. The mixture was diluted with 400 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (407 mg, 68%) as a red solid. 1H NMR (DMSO-d6)δ2.35 (s, 3H, pyrrole-CH3), 2.44 (s, 3H, pyrrole-CH3), 3.42 (m, 2H, CH2), 3.47 (m, 2H, CH2), 5.18 (s, 2H, benzene-NH2), 6.33 (m, 1H), 6.53 (m, 2H), 6.85 (m, 1H), 7.06 (m, 1H), 7.21˜7.25 (m, 2H), 7.71 (s, 1H), 7.93 (d, J=8.0 Hz, 1H), 8.33 (d, J=8.0 Hz, 1H), 8.64 (s, 2H) 9.31 (s, 1H, benzene-NH), 10.73 (s, 1H, indolinone-NH), 11.84 (s, 1H, pyrrole-NH). LC-MS (m/z) 600 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158656B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-79b36f978c9746a4b1bf747845319485 |
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| Source note | uspto-grants-2012_04 |
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