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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275886Generated: November 1, 2026

4-Methylmorpholine → HCID 86717964, compound

https://huagongshe.com/reaction/2275886

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Amino-2,2,6,6-tetramethylpiperidineHCID 37524—
Reactant8-((2,6-Difluorobenzyl)oxy)-2-methylimidazo[1,2-a]pyridine-3-carboxylic acidHCID 86717872—
ReactantHCID 178484679HCID 178484679—
SolventDimethylformamideHCID 6228—
ProductHCID 86717964HCID 86717964—

Reaction Steps

18.8 mg (0.12 mmol) of 2,2,6,6-tetramethylpiperidine-4-amine were initially charged, and 32 mg (0.10 mmol) of 8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-3-carboxylic acid in 0.4 ml of DMF and 42 mg (0.13 mmol) of (benzotriazol-1-yloxy)bisdimethylaminomethylium fluoroborate (TBTU) in 0.2 ml of DMF were added. 20 mg (0.20 mmol) of 4-methylmorpholine were then added, and the reaction was stirred at RT overnight. The mixture was then filtered off and the filtrate was purified by preparative LC-MS (Method 12). The product-containing fractions were concentrated under reduced pressure. This gave 27 mg (59% of theory) of the target product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126998B2
Source datasetuspto-grants-2015_09
ORD IDord-bf2ece3718354579a31a382cb38fc3bc
Source noteuspto-grants-2015_09