HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 59300778, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 67426354 | HCID 67426354 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59300778 | HCID 59300778 | — |
Reaction Steps
To a solution of thiophenol (70 μl) in CH2Cl2 (4 ml) is added NaH (43 mg; 1.08 mmol) and the resulting suspension is stirred for 5 min at RT. Then freshly prepared 2-chloromethyl-7,7-dimethyl-5-pentyl-5,7-dihydro-1H-imidazo[4,5-f]indol-6-one (265 mg) dissolved in CH2Cl2 (5 ml) is added and the mixture is stirred at 40° C. for 20 h. After cooling to 0° C. 3-chloro-benzenecarboperoxoic acid (186 mg; 0.83 mmol) is added and stirring is continued for another 3 h. After completion of the reaction the mixture is concentrated in vacuo and purified by NP-HPLC eluting with CH2Cl2/MeOH to give the desired compound (5.8 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714010B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-a8e17caf8e2a4f889db52749e12eaaee |
| Source note | uspto-grants-2010_05 |