Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 86685008 | HCID 86685008 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86685007 | HCID 86685007 | 50% |
Reaction Steps
N-phthaloyl protected 5-nonyloxy-4-azaindole (20 mg, 0.05 mmole) and hydrazine (3 mg, 0.09 mmole) was dissolved in CH2Cl2 (0.5 mL) in a 25 mL round bottom flask. EtOH (1 mL) was added to the reaction mixture and allowed to stir overnight at 25° C. for 12 h, after which it was cooled to 0° C., and filtered, and the white solid material was washed with 3 mL of cold CH2Cl2. The filtrate was evaporated under reduced pressure to afford 7 mg (50%) of 2-aminoethyl-5-nonyloxy-4-azaindole as a yellow solid. LRMS (ESI): M+1 for C18H29N3O calcd 304.4. found 304.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073851B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-152469a419f54f7e9dcbf9cc3ad278b4 |
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| Source note | uspto-grants-2015_07 |
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