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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586234Generated: November 1, 2026

HCID 11336372, compound → HCID 10222165, compound

https://huagongshe.com/reaction/586234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11336372HCID 11336372—
ReactantHCID 11459593HCID 11459593—
ReactantIsohexane ethyl acetateHCID 21882781—
ProductHCID 10222165HCID 10222165—

Reaction Steps

5′-(5,5-Dimethyl-[1,3,2]dioxaborinan-2-yl)-4,2′-difluorobiphenyl-2-carbonitrile was coupled to 7-bromo-3-(1-fluoro-1-methylethyl)imidazo[1,2-b][1,2,4]triazine in 77% yield using a similar procedure to that described in Example 3, step f, to give a yellow solid: mp 156-159° C. (EtOAc-isohexane); 1H NMR (400 MHz, CDCl3) δ 1.84 (6H, d, J 22.0 Hz), 7.36-7.46 (2H, m), 7.54 (1H, dd, J 7.8, 2.7 Hz), 7.57-7.60 (1H, m), 8.10-8.16 (2H, m), 8.30 (1H, s), 8.79 (1H, d, J 1.2 Hz); MS (ES+) m/z 394 [M+H]+. Anal. Found: C, 64.07; H, 3.66; N, 17.60%. Required for C21H14F3N5: C, 64.12; H, 3.59; N, 17.80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936608B2
Source datasetuspto-grants-2005_08
ORD IDord-aa439645d5854a1b96d157e0329b2a10
Source noteuspto-grants-2005_08