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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509225Generated: November 1, 2026

Ethane, 1-fluoro-2-iodo- → HCID 123982281, compound

https://huagongshe.com/reaction/1509225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthane, 1-fluoro-2-iodo-HCID 69804—
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 123982281HCID 123982281—

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 1-fluoro-2-iodoethane (111 mg, 0.636 mmol) to afford the title compound (85 mg. 1H NMR (500 MHz, CDCl3): 7.45 (1H, s), 7.24-7.31 (7H, m), 7.17-7.20 (2H, m,), 5.01 (1H, s), 4.94 (2H, s), 4.80 (1H, t), 4.70 (1H, t), 4.27 (1H, t), 4.22 (1H, t), 2.44-2.49 (4H, m), 2.06 (1H, m), 1.86 (1H, m), 1.2-1.43 (9H, br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-ef6e70dd41a14147adaf003d88565ab4
Source noteuspto-grants-2015_12