HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethoxyacetyl chloride → Tert-butyl 2-({2-chloro-3-[(ethoxyacetyl)amino]quinolin-4-yl}amino)ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethoxyacetyl chloride | HCID 84189 | — |
| Reactant | Tert-butyl 2-[(3-amino-2-chloroquinolin-4-yl)amino]ethylcarbamate | HCID 86616882 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl 2-({2-chloro-3-[(ethoxyacetyl)amino]quinolin-4-yl}amino)ethylcarbamate | HCID 86616883 | 93.1% |
Reaction Steps
A solution of ethoxyacetyl chloride (857 mg, 6.99 mmol) in acetonitrile (5 mL) was added to solution of tert-butyl 2-[(3-amino-2-chloroquinolin-4-yl)amino]ethylcarbamate (2.14 g, 6.35 mmol) in acetonitrile (20 mL). After five minutes, the solution was cooled in an ice bath and a white precipitate began to form. After one hour, the precipitate was isolated by filtration and dried under vacuum to afford the hydrochloride salt of tert-butyl 2-({2-chloro-3-[(ethoxyacetyl)amino]quinolin-4-yl}amino)ethylcarbamate (2.50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915281B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-87c4883a99a14edc9dbb2b0855d5d17d |
| Source note | uspto-grants-2011_03 |