HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(7-Benzyloxy-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Propanol, 1-amino-2-methyl- | HCID 95102 | — |
| Reactant | 7-(Benzyloxy)-4-chloro-3-nitroquinoline | HCID 21075751 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(7-Benzyloxy-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol | HCID 67051017 | 77.8% |
Reaction Steps
7-Benzyloxy-4-chloro-3-nitroquinoline (66.4 g, 0.21 mol) was dissolved in a mixture of dichloromethane (1.5 L) and triethylamine (59 mL, 0.422 mol). A solution of 1-amino-2-methyl-2-propanol (22.5 g, 0.25 mol) in dichloromethane (100 mL) was added dropwise. The reaction was stirred at ambient temperature for 3 hours and then quenched with 1% aqueous sodium carbonate solution. A precipitate formed which was filtered to provide 60 g of crude 1-(7-benzyloxy-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol as a yellow-brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08263594B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-42c77b53272b4a13a656799909b4911b |
| Source note | uspto-grants-2012_09 |