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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175036Generated: November 1, 2026

2-Chlorobenzoxazole → HCID 52915314, compound

https://huagongshe.com/reaction/2175036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactant2-ChloroquinoxalineHCID 238938—
ReactantHCID 67086559HCID 67086559—
ReactantHCID 67086667HCID 67086667—
ProductHCID 52915314HCID 52915314—

Reaction Steps

The title compound was prepared in a manner analogous to Example 1, substituting the trifluoro acetic acid salt of (3,8-diaza-bicyclo[4.2.0]oct-8-yl)-(2,6-dimethoxy-phenyl)-methanone (Intermediate 4) for biphenyl-2-yl-(3,8-diaza-bicyclo[4.2.0]oct-8-yl)methanone and 2-chlorobenzoxazole for 2-chloro quinoxaline. MS (ESI) mass calcd. for C22H23N3O3, 393.45; m/z found, 394.0 [M+H]+. 1H NMR (CDCl3): 7.54-7.26 (m, 3H), 7.24-7.10 (m, 2H), 7.08-7.02 (m, 0.6H), 6.80-6.73 (m, 0.4H), 6.33-6.22 (m, 1H), 4.74-4.64 (m, 1H), 4.14-3.56 (m, 5H), 3.50-3.35 (m, 1H), 2.99-2.85 (m, 1H), 2.72-2.56 (m, 1H), 2.36-2.20 (m, 5H), 2.03-1.78 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062044B2
Source datasetuspto-grants-2015_06
ORD IDord-c9b2ac09915b4ea89beadf0dcb281a12
Source noteuspto-grants-2015_06