HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → ethyl 6-bromo-4-[[(2S)-2-methoxypropyl]amino]quinoline-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 6-bromo-4-chloroquinoline-3-carboxylate | HCID 2764138 | — |
| Reactant | (S)-2-Methoxypropan-1-amine hydrochloride | HCID 71607326 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 6-bromo-4-[[(2S)-2-methoxypropyl]amino]quinoline-3-carboxylate | HCID 68108432 | — |
Reaction Steps
Suspend ethyl-6-bromo-4-chloro-quinoline-3-carboxylate (389 g, 1.24 mol) and (2S)-2-methoxypropan-1-amine, hydrochloride (171 g, 1.36 mol, 1.1 eq.) in ethanol (5.84 L). Add diisopropylethylamine (474 mL) and heat the mixture at 50° C. overnight. After 16 hours, cool the reaction to room temperature and concentrate in vacuo. Add methyl tert-butyl ether (2 L) to the residue and stir for 20 min. Filter the precipitate and wash it with methyl tert-butyl ether (2×250 mL). Concentrate the filtrate in vacuo to afford the titled compound in almost quantitative yield. The compound will be used in the next step without further purification. MS (ESI) m/z (M+H)+ 367.0, 369.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658668B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-6d5fa84e05894992a374e5e996b82bd8 |
| Source note | uspto-grants-2014_02 |