HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842059Generated: November 3, 2026
Diisopropylethylamine → 5-benzyl-1-methyl-N-(3-(pyridin-4-yl)-1-trityl-1H-indazol-5-yl)piperidine-3-carboxamide
https://huagongshe.com/reaction/1842059
Participants
| Role | Name | HCID | Charge |
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| 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-(pyridin-4-yl)-1-trityl-1H-indazol-5-amine | HCID 57685810 | — |
| Reactant | 5-Benzyl-1-methylpiperidine-3-carboxylic acid | HCID 66609252 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-benzyl-1-methyl-N-(3-(pyridin-4-yl)-1-trityl-1H-indazol-5-yl)piperidine-3-carboxamide | HCID 66614586 | — |
Reaction Steps
2-(7-Aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU) (0.11 mmol) was added to a suspension of 5-benzyl-1-methylpiperidine-3-carboxylic acid (0.1 mmol) in DMF (0.5 mL) and was stirred at room temperature for 15 minutes. A solution of 3-(pyridin-4-yl)-1-trityl-1H-indazol-5-amine (0.1 mmol) in DMF (0.5 mL) was added to the reaction and followed by diisopropyl ethyl amine (DIEA) (0.1 mL). The mixture was stirred at room temperature for an additional 30 minutes. The reaction was quenched with water (5 mL) and extracted with ethyl acetate (3×10 mL). The extracts were combined, dried using anhydrous sodium sulfate, filtered, and concentrated in vacuo. The crude product was progressed to the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946216B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-634d74eee42e44ea81b710ece6597ffa |
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| Source note | uspto-grants-2015_02 |
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