HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275882Generated: October 31, 2026
4-Methylmorpholine → HCID 86717961, compound
https://huagongshe.com/reaction/2275882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 2-Methylpropylenediamine | HCID 13128 | — |
| Reactant | 8-((2,6-Difluorobenzyl)oxy)-2-methylimidazo[1,2-a]pyridine-3-carboxylic acid | HCID 86717872 | — |
| Reactant | HCID 178484679 | HCID 178484679 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86717961 | HCID 86717961 | — |
Reaction Steps
100 mg of 8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-3-carboxylic acid (0.31 mmol), 151 mg of (benzotriazol-1-yloxy)bisdimethylaminomethylium fluoroborate (TBTU, 0.47 mmol) and 127 mg of 4-methylmorpholine (1.26 mmol) were initially charged in 2 ml of DMF. 55 mg of 2-methylpropane-1,2-diamine (0.63 mmol) were then added, and the mixture was stirred at RT overnight. The reaction solution was purified by preparative HPLC (RP18 column, mobile phase: acetonitrile/water gradient with addition of 0.1% TFA). The crude product was taken up in ethyl acetate and washed twice with saturated aqueous sodium bicarbonate solution. The aqueous phase was extracted twice with ethyl acetate and the combined organic phases were dried over sodium sulphate. The mixture was then filtered and the filtrate was concentrated and lyophilized. This gave 80 mg of the title compound (66% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126998B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-6299068ffebd4ee7bc279ab65f21f55b |
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| Source note | uspto-grants-2015_09 |
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