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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-(pyridin-4-yl)-1-trityl-1H-indazol-5-amineHCID 57685810—
Reactant5-Benzyl-1-methylpiperidine-3-carboxylic acidHCID 66609252—
SolventDimethylformamideHCID 6228—
Product5-benzyl-1-methyl-N-(3-(pyridin-4-yl)-1-trityl-1H-indazol-5-yl)piperidine-3-carboxamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946216B2
Source datasetuspto-grants-2015_02
ORD IDord-634d74eee42e44ea81b710ece6597ffa
Source noteuspto-grants-2015_02