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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509183Generated: October 31, 2026

4-Bromobutyronitrile → HCID 123768507, compound

https://huagongshe.com/reaction/1509183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobutyronitrileHCID 21412—
ReactantHCID 67256382HCID 67256382—
Reactanttert-butyl(1-(4-(1-(2-cyanoethyl)-2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutyl)carbamateHCID 123769430—
ProductHCID 123768507HCID 123768507—

Reaction Steps

Following the procedure for tert-butyl(1-(4-(1-(2-cyanoethyl)-2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutyl)carbamate, tert-butyl 1-(4-(2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutylcarbamate (100 mg, 0.212 mmol) was reacted with 4-bromobutanenitrile (94 mg, 0.636 mmol) to afford the title compound (68 mg. 1H NMR (500 MHz, CDCl3): 7.20-7.32 (10H, m), 5.1 (1H, br), 4.90 (2H, s), 4.11 (2H, m), 2.44-2.50 (6H, m), 2.05-2.13 (3H, m), 1.79-1.84 (1H, m), 1.27-1.36 (9H, br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-decc73fef42b4aea8e2d9139c3cff375
Source noteuspto-grants-2015_12