HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174283Generated: October 30, 2026
Morpholine → 4-(2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)pyridin-4-yl)morpholine
https://huagongshe.com/reaction/2174283
Participants
| Role | Name | HCID | Charge |
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| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-(3-(4-bromopyridin-2-yl)-1-(2-fluorobenzyl)-1H-1,2,4-triazol-5-yl)thiazole | HCID 69094285 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Ethylene glycol dioxane | HCID 22419261 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 4-(2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)pyridin-4-yl)morpholine | HCID 69092145 | 79% |
Reaction Steps
To a stirring suspension of 2-(3-(4-bromopyridin-2-yl)-1-(2-fluorobenzyl)-1H-1,2,4-triazol-5-yl)thiazole (I-36, 1 eq) and copper(I) oxide (1 eq) in ethylene glycol-dioxane (approx. 4:1) in a sealed tube is added morpholine (30 eq). The resultant reaction mixture was heated at 100° C. for 12 hr. The reaction was cooled to room temperature and treated with brine and then extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated and purified using SiO2 chromatography (methylene chloride/acetonitrile/methanol) to afford 4-(2-(1-(2-fluorobenzyl)-5-(thiazol-2-yl)-1H-1,2,4-triazol-3-yl)pyridin-4-yl)morpholine as a solid in 79% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09061030B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-51ffc228cc0549c28e2c9673b26c6412 |
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| Source note | uspto-grants-2015_06 |
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