HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 131726650, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 69410956 | HCID 69410956 | — |
| Reactant | HCID 131726651 | HCID 131726651 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131726650 | HCID 131726650 | — |
Reaction Steps
A solution of 4-fluorobenzoyl-azetidine hydrochloride (0.192 g, 0.892 mmol), triethylamine (0.252 ml, 3.24 mmol) and [(S)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-iodo-propyl]-carbamic acid tert-butyl ester (0.448 g, 0.811 mmol) in dimethylformamide (3 ml) is stirred at ambient temperature for 18 hours, then partitioned between ethylacetate and water. The ethylacetate phase is dried over MgSO4 and evaporated. The crude product is purified by flash silica chromatography (elution with a 1:99 methanol/dichloromethane) to afford {(S)-1-(tert-butyl-diphenyl-silanyloxymethyl)-3-[3-(4-fluoro-benzoyl)-azetidin-1-yl]-propyl}carbamic acid tert-butyl ester. [MH]+ 605.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07288537B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-a347f5e56bcc47d8bfc822db4552cdee |
| Source note | uspto-grants-2007_10 |