HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383110Generated: November 3, 2026
tert-butyl N-(4-aminobutyl)carbamate → HCID 69027554, compound
https://huagongshe.com/reaction/2383110
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-(Benzyloxy)-4-chloro-3-nitroquinoline | HCID 21075751 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 69027554 | HCID 69027554 | 73.2% |
Reaction Steps
tert-Butyl N-(4-aminobutyl)carbamate (22.01 g, 116.9 mmol) was added to a solution of 7-benzyloxy-4-chloro-3-nitroquinoline (36.80 g, 116.9 mmol), prepared in Parts A-D of Example 1, in distilled water. The reaction was heated at 80° C. for 1.5 hours and then stirred at room temperature for four hours. The reaction was not complete, and triethylamine (16 mL, 115 mmol) was added. The reaction was stirred overnight at room temperature. A precipitate formed, which was isolated by filtration and washed with hexanes to provide 39.92 g of tert-butyl[4-(7-benzyloxy-3-nitroquinolin-4-ylamino)butyl]carbamate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263594B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-d61ae5288608495f919d50db34618e5d |
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| Source note | uspto-grants-2012_09 |
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