HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099351Generated: November 1, 2026
Sodium triacetoxyborohydride → HCID 68828337, compound
https://huagongshe.com/reaction/2099351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl 2-oxopiperidine-1-carboxylate | HCID 7577838 | — |
| Reactant | HCID 68829063 | HCID 68829063 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68828337 | HCID 68828337 | 65.6% |
Reaction Steps
0.41 g of N-[8-(4-chloro-D-phenylalanyl)-8-azabicyclo[3.2.1]oct-3-yl]-N-cyclohexyl-N′,N′-diethylurea is dissolved in 4 ml of dichloromethane under N2 in the presence of 0.17 g of N-BOC-piperidone and of 0.23 g of sodium triacetoxyborohydride, and the mixture is stirred at ambient temperature for 16 h. After evaporation and hydrolysis, extraction is carried out with ethyl acetate until the aqueous phase is completely depleted. The organic phase is washed with H2O and then with a saturated aqueous sodium chloride solution. Drying over MgSO4 and concentration to dryness are carried out. The crude is chromatographed on silica gel, elution being carried out with a 98/2 mixture of dichloromethane and methanol. 0.37 g of tert-butyl 4-{[(1R)-1-(4-chlorobenzyl)-2-(3-{cyclohexyl[(diethylamino)carbonyl]amino}-8-azabicyclo-[3.2.1]oct-8-yl)-2-oxoethyl]amino}piperidine-1-carboxylate is then obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569582B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-0b5e6f590b2b48d39c628b6a42fe775f |
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| Source note | uspto-grants-2009_08 |
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