HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 86650281, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-((tert-Butoxycarbonyl)amino)hexanoic acid | HCID 637602 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | Tenovin-3 | HCID 24772097 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86650281 | HCID 86650281 | 54% |
Reaction Steps
Thiourea 4 (100 mg, 0.31 mmol, 1 equiv.) was stirred in dry CH2Cl2 (5 mL) under N2 atmosphere and acid 31 (106 mg, 0.46 mmol, 1.5 equiv.) was added, followed by bromo-tris-pyrrolidino phosphoniumhexafluorophosphate (214 mg, 0.46 mmol, 1.5 equiv.), and N,N-diisopropylethylamine (53 μL, 0.31 mmol, 1 equiv.). The reaction mixture was stirred at rt for 16 h then diluted with CH2Cl2 (20 mL) and washed with 1 M aqueous hydrochloric acid (1×10 mL), 1 M aqueous sodium hydroxide (1×10 mL), and saturated brine (1×10 mL). The organic phase was dried over MgSO4 and concentrated in vacuo to give a crude yellow oil which was purified with column chromatography on silica (25-50% ethyl acetate/petroleum ether) to give 32 (86 mg, 54%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501991B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-a85a7685852241df9725fc8904fec06a |
| Source note | uspto-grants-2013_08 |