HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 59703629, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | HCID 59703623 | HCID 59703623 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59703629 | HCID 59703629 | 33.4% |
Reaction Steps
At room temperature, 6′-Chloro-3′-(3-chloro-benzyl)-2-(morpholine-4-carbonyl)-2,3,1′,3′-tetrahydro-[1,3′]biindolyl-2′-one (60 mg, 0.115 mmol) and DDQ (47 mg, 0.207 mmol) were dissolved in 5 ml toluene. After stirred overnight, the solution was concentrated and then the residue was dissolved in EtOAc. The organic layer was washed with 10% NaOH aqueous solution and dried, concentrated to obtain crude product. The crude product was purified by chromatography to obtain 20 mg yellow solid rac-6′-Chloro-3′-(3-chloro-benzyl)-2-(morpholine-4-carbonyl)-1′,3′-dihydro-[1,3′]biindolyl-2′-one. MS: 520 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058269B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-ad9e69ee7bc64dd8a75abd523ee4c913 |
| Source note | uspto-grants-2011_11 |