HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203538Generated: November 1, 2026
Acetyl chloride → N-[1,1-dimethyl-2-(3-nitro-7-benzyloxyquinolin-4-ylamino)ethyl]acetamide
https://huagongshe.com/reaction/2203538
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2-Amino-2-methylpropyl)(7-benzyloxy-3-nitroquinolin-4-yl)amine | HCID 67050934 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[1,1-dimethyl-2-(3-nitro-7-benzyloxyquinolin-4-ylamino)ethyl]acetamide | HCID 68897784 | — |
Reaction Steps
Under a nitrogen atmosphere, a solution of (2-amino-2-methylpropyl)(7-benzyloxy-3-nitroquinolin-4-yl)amine (6.5 g, 17.5 mmol), prepared in Part A of Example 45, in dichloromethane (200 mL) was cooled to 0° C.; triethylamine (4.87 mL, 35.0 mmol) and acetyl chloride (1.37 mL, 19.2 mmol) were sequentially added. The reaction was stirred at 0° C. for 30 minutes, allowed to warm to ambient temperature, and stirred for three hours. The reaction was washed with saturated aqueous sodium bicarbonate (2×) and brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide N-[1,1-dimethyl-2-(3-nitro-7-benzyloxyquinolin-4-ylamino)ethyl]acetamide as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365567B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-80d32900af044267a0de402e5bf05855 |
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| Source note | uspto-grants-2016_06 |
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