HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154946Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 20563557, compound
https://huagongshe.com/reaction/1154946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Benzenemethanamine, N-cyclohexyl- | HCID 204463 | — |
| Reactant | HCID 12819300 | HCID 12819300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20563557 | HCID 20563557 | 23.9% |
Reaction Steps
To a solution of 2.9 g of 5-(6-carboxyhexyloxy)-3,4-dihydrocarbostyril and 1.9 g of N-benzylcyclohexylamine in 100 ml of DMF is added gradually dropwise a solution of 2.1 g of N,N'-dicyclohexylcarbodiimide in 10 ml of DMF at room temperature and under agitation. After this agitation, the mixture is further agitated at room temperature for 5 hours. After the reaction, the insolubles are filtered off and the mother liquor is concentrated. The residue is dissolved in chloroform and subjected to silica gel thin-layer chromatography (solvent: chloroform-methanol (8:1) to scrape out the portion with Rf value of 0.8. The silica gel is extracted with chloroform, and after distilling off chloroform, the residue is recrystallized from benzene-ligroin to obtain 1.1 g of 5-[6-(N-cyclohexyl-N-benzylaminocarbonyl)hexyloxy]-3,4-dihydrocarbostyril in the form of colorless needle-like crystals with melting point of 49°-52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04298739 |
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| Source dataset | uspto-grants-1981_11 |
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| ORD ID | ord-add44c1406b14d88bdea036fe2dcc5e0 |
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| Source note | uspto-grants-1981_11 |
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