Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373947Generated: October 31, 2026

Triethylamine → HCID 21075826, compound

https://huagongshe.com/reaction/1373947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl carbazateHCID 70091—
Reactant7-Bromo-4-chloro-3-nitroquinolineHCID 21984361—
SolventDichloromethaneHCID 6344—
ProductHCID 21075826HCID 21075826100%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 7-bromo-4-chloro-3-nitroquinoline (75.00 g, 260.9 mmol) in 350 mL of dichloromethane was cooled to 0° C. under an atmosphere of nitrogen. The suspension was treated with triethylamine (43.25 mL, 326.1 mmol), which dissolved most of the material. A solution of tert-butyl carbazate (37.93 g, 287.0 mmol) in 250 mL of dichloromethane was added to the reaction mixture over 20 min. The reaction was allowed to slowly come to ambient temperature. After 15 h, the reaction mixture was washed with 5% Na2CO3 solution (2×100 mL) and water (100 mL). The combined aqueous washes were back-extracted with CHCl3 (50 mL). The combined organic portions were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated under reduced pressure to yield 99.98 g of tert-butyl N′-(7-bromo-3-nitroquinolin-4-yl)hydrazinecarboxylate as a dark red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163947B2
Source datasetuspto-grants-2007_01
ORD IDord-0044cd813efe4dc8b1f05fc5577ef446
Source noteuspto-grants-2007_01