HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-(Trifluoromethyl)benzylic alcohol → 2-(Trifluoromethyl)benzyl 7-bromo-3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-(Trifluoromethyl)benzylic alcohol | HCID 67666 | — |
| Edukt | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| Edukt | 7-bromospiro[indene-1,4'-piperidin]-3(2H)-one | HCID 58295671 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-(Trifluoromethyl)benzyl 7-bromo-3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylate | HCID 44227079 | — |
Reaktionsschritte
To o-(trifluoromethyl)benzyl alcohol (35 mg, 0.20 mmol) in CH2Cl2 (4 mL) was added was a solution of carbonyl diimidazole (29 mg, 0.18 mmol) in CH2Cl2 (4 mL). The mixture was stirred at rt for 2 h. A 1-mL aliquot of the resulting solution (0.05 mmol) was added to a solution 7-bromospiro[indene-1,4′-piperidin]-3(2H)-one (14.5 mg, 0.05 mmol) in CH2Cl2 (1 mL). The mixture was stirred at rt for 16 h, concentrated, redissolved in MeCN (1 mL) and heated at 60° C. for 2 h. Prep HPLC afforded the title compound. LC-MS Method 1 tR=2.06, min, m/z=484, 482.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08383629B2 |
| Quelldatensatz | uspto-grants-2013_02 |
| ORD ID | ord-67ab8ad46ead4b3d99d43255073f14ae |
| Quellennotiz | uspto-grants-2013_02 |