HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzoyl chloride → HCID 46843218, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 66677239 | HCID 66677239 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 46843218 | HCID 46843218 | — |
Reaction Steps
3-Chloro-6,7,8,9-tetrahydro-5H-dipyrido[2,3-b;3′,4′-d]pyrrole (50 mg, 0.24 mmol) and DIEA (0.05 L, 0.29 mmol) were dissolved in THF (2 ml) and stirred at room temperature. 4-Chlorobenzoyl chloride (0.04 mL, 0.29 mmol) was added dropwise, and the reaction was stirred for 1 h at room temperature. The reaction was quenched with H2O (200 mL). The resulting precipitate was filtered, and dried overnight under vacuum. The HCl salt was formed via dissolving the precipitate in MeOH (2 ml) and adding 1 M HCl/ether (2 equivalents), and cooling at 0° C. overnight. The resulting precipitate was filtered, and dried under vacuum to provide 18 (54 mg, 59% yield) as a yellow powder. LC-MS (M+H=346, obsd.=346).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853391B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-bf7e0fdbb4704a1da93fc5fc26bfa9ef |
| Source note | uspto-grants-2014_10 |