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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786116Generated: November 1, 2026

4-Methylmorpholine → N-[(2R)-2-({2-[4-(3-Buten-1-yl)-6-(dimethylamino)-1,3,5-triazin-2-yl]hydrazino}carbonyl)-7-octen-1-yl]-N-benzoxyformamide

https://huagongshe.com/reaction/1786116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(3-Buten-1-yl)-6-(dimethylamino)-2-hydrazino-1,3,5-triazineHCID 68848123—
Reactant(2R)-2-({N-formyl-N-benzoxy-amino}methyl)-7-octenoic acidHCID 86621282—
SolventDimethylformamideHCID 6228—
ProductN-[(2R)-2-({2-[4-(3-Buten-1-yl)-6-(dimethylamino)-1,3,5-triazin-2-yl]hydrazino}carbonyl)-7-octen-1-yl]-N-benzoxyformamideHCID 86621283—

Reaction Steps

To a mixture of (2R)-2-({N-formyl-N-benzoxy-amino}methyl)-7-octenoic acid (233 mg, 1.121 mmol), 4-(3-buten-1-yl)-6-(dimethylamino)-2-hydrazino-1,3,5-triazine (342 mg, 1.121 mmol), NMM (0.62 mL, 5.61 mmol) and HOAt (183 mg, 1.345 mmol) in DMF (11 mL) at room temperature was added 1-[3-(dimethylamino)-propyl]-3-ethylcarbodiimide hydrochloride (258 mg, 1.345 mmol). After stirring at room temperature overnight, the reaction mixture was then purified by HPLC to afford the title compound as a white solid. MH+496.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507726B2
Source datasetuspto-grants-2009_03
ORD IDord-d5ad093626464c57994b39f46b92ea52
Source noteuspto-grants-2009_03