HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855673Generated: October 30, 2026
Diisopropylethylamine → HCID 178468423, compound
https://huagongshe.com/reaction/1855673
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | 1-{1-[(R)-2-amino-3-(4-methoxyphenyl)propionyl]-4-cyclohexylpiperidin-4-yl}butan-1-one | HCID 66987681 | — |
| Reactant | HCID 178510967 | HCID 178510967 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178468423 | HCID 178468423 | 13.7% |
Reaction Steps
16 μL of diisopropylethylamine and 10 mg (51 μmol) of 4-nitrophenyl chloroformate are added to 25 mg (47 μmol) of 1-{1-[(R)-2-amino-3-(4-methoxyphenyl)propionyl]-4-cyclohexylpiperidin-4-yl}butan-1-one (cf. preparation 4.4) dissolved in 5 ml of DCM. The reaction mixture is stirred for 2 hours at room temperature. The reaction is stopped by adding water and the organic compounds are extracted with DCM. The organic phase is then dried over MgSO4, filtered and concentrated. The oil obtained is dissolved in 5 ml of DMF at 80° C., and 14 mg of 5-(1H-imidazol-4-yl)pentylamine bis(trifluoroacetate) are added. The reaction mixture is stirred at 80° C. for 5 minutes and for 18 hours at room temperature. The organic phase is washed with 1N sodium hydroxide, extracted with dichloromethane and then dried over MgSO4, filtered and concentrated. The crude product obtained is purified by preparative HPLC. 3 mg of ethyl 4-cyclohexyl-1-[(R)-2-{3-[5-(1H-imidazol-4-yl)pentyl]ureido}-3-(4-methoxy-phenyl)propionyl]piperidine-4-carboxylate are obtained in a yield of 10%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962846B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-8d5ec75034094f21a684d0e42cbc57cf |
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| Source note | uspto-grants-2015_02 |
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