Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | HCID 68747834 | HCID 68747834 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11584572 | HCID 11584572 | 102.7% |
Reaction Steps
4-Fluorobenzoyl chloride (111 mg, 0.7 mmol) was added to a solution of N′-[5-(1H-indol-5-yl)-pyridin-3-ylmethyl]-N,N-dimethyl-ethane-1,2-diamine (160 mg, 0.54 mmol) and triethyl amine (109 mg, 1.08 mmol) in 15 mL of dichloromethane at room temperature. The resulting mixture was stirred at ambient temperature overnight, and then a further 111 mg of 4-fluorobenzoyl chloride was added and the mixture stirred for an additional 2 h. The volatiles were removed in vacuo to leave the crude product. Chromatography (elution with methanol/dichloromethane) provided 231 mg of material. This was dissolved in dichloromethane and washed with 1M sodium hydroxide solution. The organic phase was dried over magnesium sulfate, filtered and concentrated to leave material which was further purified by HPLC (elution with acetonitrile/water/TFA) to give 21 mg of product. LC/MS (long run): Retention time, 3.85 min; (M+H)=417.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07625889B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-57676dd72f014663a4384d2ef4c32727 |
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| Source note | uspto-grants-2009_12 |
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