HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565661Generated: October 29, 2026
Benzhydrylamine → HCID 22110990, compound
https://huagongshe.com/reaction/565661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzhydrylamine | HCID 7036 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 23667828 | HCID 23667828 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22110990 | HCID 22110990 | 57% |
Reaction Steps
To a suspension of sodium 1-[(5-amino-2,4,6,7-tetramethyl-2,3-dihydrobenzofuran-2-yl)methyl]-4-piperidinecarboxylate (0.89 g) in N,N-dimethylformamide (10 mL) was added 0.35 g of triethylamine hydrochloride and the mixture was stirred at room temperature for 5 minutes. To this mixture were added 0.34 g of 1-hydroxybenzotriazole and 0.46 g of 1,1-diphenylmethylamine. Then, under ice-cooling, 0.48 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added. This mixture was stirred under nitrogen gas at room temperature for 23 hours. This reaction mixture was diluted with water and extracted with 2 portions of ethyl acetate. The pooled organic layer was washed with water and saturated aqueous NaCl, dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was recrystallized from methanol/diisopropyl ether to provide 0.71 g of the title compound. Yield 57%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172085B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-1da96b5c3f294d37b73dc207e7fca655 |
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| Source note | uspto-grants-2001_01 |
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