HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 178453969, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 1,7-Diphenyl-4-aminoheptane hydrochloride | HCID 21892255 | — |
| Reactant | HCID 178453971 | HCID 178453971 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178453969 | HCID 178453969 | — |
Reaction Steps
N-(tert-Butoxycarbonyl)-cis-4-amino-1-cyclohexanecarboxylic acid (23) (1.00 g; 4.11 mmol) is dissolved in methylene chloride (30 mL) at ambient temperature. 1,7-Diphenyl-4-aminoheptane hydrochloride (1) (1.50 g; 4.93 mmol), N,N-diisopropylethylamine (1.70 g; 13.15 mmol) and PyBOP (2.57 g; 4.93 mmol) are added sequentially. The reaction is stirred 4 hours at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography (20%→40% ethyl acetate in hexanes) affording the desired product as a solid. CIMS: MH+ 493
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06693099B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-e6befaa4fda74bb596108644535cc4d2 |
| Source note | uspto-grants-2004_02 |