HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 46843683, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 66677889 | HCID 66677889 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 46843683 | HCID 46843683 | 26% |
Reaction Steps
(6,7,8,9-Tetrahydro-5H-dipyrido[2,3-b;3′,4′-d]pyrrol-4-yl)-(5,6,7,8-tetrahydro-naphthalen-2-yl)-amine (75 mg, 0.24 mmol), acetic anhydride (25 μL, 0.24 mmol), and triethylamine (98 μL, 0.71 mmol) were dissolved in 1,2-dichloroethane (2 mL), and stirred for 30 min at room temperature. The reaction was quenched with H2O, and the resulting material was filtered through an Extrelut column. The Extrelut column was washed with EtOAc, and the filtrate was concentrated. The crude material was purified via Biotage eluting with a gradient of 0 to 10% MeOH in DCM. Lyophilization of the purified product provided 59 (22 mg, 26% yield) as a tan powder. LC-MS (M+H=361, obsd.=361).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853391B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-eace92e413f342c9973c6fc000abe934 |
| Source note | uspto-grants-2014_10 |