HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → HCID 131729181, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | HCID 131729182 | HCID 131729182 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131729181 | HCID 131729181 | 87.1% |
Reaction Steps
607 mg Boc-Dap(Fmoc)-N-lauryl-N-myristyl amide were dissolved in 8 ml anhydrous dichloromethane in a 50 ml round-bottom flask (FIG. 6). 3 ml diethylamine were added and the reaction steered at room temperature for 4.5 hours. The volatile constituents were removed using a rotary evaporator and the residue was purified by chromatography using 40 g silica gel 60 (Merck) with hexane/ethylacetate 5:1. The product was eluted by a step gradient consisting of ethylacetate, dichloromethane and dichloromethane/methanol 3:1. 372 mg (0.655 mmol) Boc-Dap-N-lauryl-N-myristyl amide were obtained as yellowish, viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09387262B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-a7e1a846a1234a578c5b5d48bd20410f |
| Source note | uspto-grants-2016_07 |