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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109994Generated: October 31, 2026

Diisopropylcarbodiimide → HCID 10195903, compound

https://huagongshe.com/reaction/2109994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantN-Acetyl-beta-alanineHCID 76406—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 69070294HCID 69070294—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10195903HCID 10195903—

Reaction Steps

After dissolving 4-amino-2-[(1-naphthalen-1-ylmethyl-piperidin-4-ylmethyl)-amino]-benzimidazole-1-carboxylic acid tert-butyl ester (0.02 mmol) in tetrahydrofuran (1 ml), diisopropylcarbodiimide (0.05 mmol), 1-hydroxybenzotriazole monohydrate (0.05 mmol) and 3-acetylaminopropionic acid (0.05 mmol) were added and the mixture was stirred at room temperature overnight. After adding a 4N hydrogen chloride-1,4-dioxane solution (1 ml) to the reaction mixture, it was stirred at 50° C. for 1 hour, the solvent was removed under reduced pressure, and then dichloromethane and 5N aqueous sodium hydroxide were added to the obtained residue prior to stirring. The organic layer was passed through SCX (Bond Elute SCX500MG), and after washing the SCX with methanol, elution was performed with a 2N ammonia-methanol solution. The solvent was distilled off under reduced pressure to obtain 3-acetylamino-N-{2-[(1-naphthalen-1-ylmethyl-piperidin-4-ylmethyl)-amino]-1H-benzimidazol-4-yl}-propionamide. The compound was identified by LC-MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517875B2
Source datasetuspto-grants-2009_04
ORD IDord-0eb8d853a341444c9cce3c59d634fe03
Source noteuspto-grants-2009_04