HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30792Generated: October 26, 2026
Triethylamine → n-{4-[4-(Methylamino)-3-nitrophenoxy](2-pyridyl)}[(2-morpholin-4-ylethyl)amino]carboxamide
https://huagongshe.com/reaction/30792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2-Morpholinoethylamine | HCID 408285 | — |
| Reactant | 4-[4-(Methylamino)-3-nitrophenoxy]pyridine-2-carboxylic acid | HCID 22040497 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | n-{4-[4-(Methylamino)-3-nitrophenoxy](2-pyridyl)}[(2-morpholin-4-ylethyl)amino]carboxamide | HCID 59790251 | — |
Reaction Steps
A flame dried flask was charged with 4-[4-(methylamino)-3-nitrophenoxy]-pyridine-2-carboxylic acid (1 eq), diphenylphosphoryl azide (1.1 eq), triethylamine (2.1 eq) and 20 ml toluene and heated for one and one half hours at 75° C. To this was added 2-morpholin-4-ylethylamine (1.2 eq) and the resulting mixture was stirred at 75° C. overnight. The reaction was then concentrated and partitioned between ethyl acetate and distilled water. The organic layer was dried with sodium sulfate and concentrated and titurated with ether then hexanes to give the purified product. MS: MH+=417.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423150B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-3cf4e63b45724422b2cfe7696403c629 |
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| Source note | uspto-grants-2008_09 |
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