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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
ReactantTriethylamineHCID 8471—
Reactant7-(Benzyloxy)-4-chloro-3-nitroquinolineHCID 21075751—
SolventWaterHCID 962—
ProductHCID 69027554HCID 6902755473.2%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263594B2
Source datasetuspto-grants-2012_09
ORD IDord-d61ae5288608495f919d50db34618e5d
Source noteuspto-grants-2012_09