Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | 5-methoxy-6-nitro-2,3-dihydro-1H-indole | HCID 59441656 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59442033 | HCID 59442033 | 100% |
Reaction Steps
A mixture of 5-(methyloxy)-6-nitro-2,3-dihydro-1H-indole (Intermediate B99, 433 mg, 2.23 mol), bromoacetyl chloride (386 mg, 2.45 mmol) and K2CO3 (924 mg, 6.69 mmol) in THF (50 mL) was stirred for 40 min and then Et2NH (326 mg, 4.46 mmol) was added. The reaction mixture was stirred for 1 day, additional Et2NH (0.3 mL) was added, stirring was continued for an additional 24 h, then the reaction was heated at 60° C. for 2 h. The resulting mixture was diluted with EtOAc (200 mL), washed with water (150 mL) and a saturated NaCl solution (100 mL), and back extracted with EtOAc (100 mL). The organic layers were combined, dried (Na2SO4), and concentrated to obtain N,N-diethyl-2-[5-(methyloxy)-6-nitro-2,3-dihydro-1H-indol-1-yl]-2-oxoethanamine (687 mg, 100%). ESIMS (M+H)+=307.97.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981903B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-fa266c7a725c4ac2a3e0d096008477e7 |
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| Source note | uspto-grants-2011_07 |
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