HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415474Generated: October 28, 2026
Water → Tert-butyl 3-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}benzylcarbamate
https://huagongshe.com/reaction/415474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-butyl N-((3-(aminomethyl)phenyl)methyl)carbamate | HCID 2756043 | — |
| Reactant | 2,4-Dichloro-3-nitroquinoline | HCID 2785138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 3-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}benzylcarbamate | HCID 86633722 | 115.2% |
Reaction Steps
Triethylamine (12.5 mL, 0.0889 mol) and 1-(N-Boc-aminomethyl)-3-(aminomethyl)benzene (17.71 g, 74.94 mmol) were sequentially added to a solution of 2,4-dichloro-3-nitroquinoline (18.2 g, 0.0750 mol) in DMF (90 mL), and the reaction was stirred at room temperature under nitrogen for 1.5 hours. The reaction was poured into water (2 L), and the suspension was stirred for 15 minutes. Most of the water was decanted away from the resulting precipitate, which was dissolved in ethyl acetate (600 mL). The ethyl acetate was separated from a small amount of remaining water and then removed under reduced pressure. The resulting solid was dried under vacuum to provide 38.24 g of tert-butyl 3-{[(2-chloro-3-nitroquinolin-4-yl)amino]methyl}benzylcarbamate as a sticky, amber solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08088790B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-a29fa9796cda4623928c8ddbffcd198f |
|---|
| Source note | uspto-grants-2012_01 |
|---|