HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109994Generated: October 31, 2026
Diisopropylcarbodiimide → HCID 10195903, compound
https://huagongshe.com/reaction/2109994
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | N-Acetyl-beta-alanine | HCID 76406 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 69070294 | HCID 69070294 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10195903 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517875B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-0eb8d853a341444c9cce3c59d634fe03 |
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| Source note | uspto-grants-2009_04 |
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