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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193187Generated: October 31, 2026

2-(Thiophen-2-yl)benzoic acid → HCID 67116977, compound

https://huagongshe.com/reaction/1193187

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Thiophen-2-yl)benzoic acidHCID 5105623—
Reactant2-(2H-1,2,3-Triazol-2-yl)benzoic acidHCID 21313592—
Reactant2-((1R,6S)-3,8-Diazabicyclo[4.2.0]octan-8-yl)-5-chlorobenzo[d]oxazoleHCID 67116781—
Reactant(1R,6S)-8-(4,6-Dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octaneHCID 68156939—
SolventDichloromethaneHCID 6344—
ProductHCID 67116977HCID 67116977—

Reaction Steps

The title compound was prepared in a manner analogous to Example 1, substituting 2-((1R,6S)-3,8-diazabicyclo[4.2.0]octan-8-yl)-5-chlorobenzo[d]oxazole (Intermediate 32) for (1R,6S)8-(4,6-dimethyl-pyrimidin-2-yl)-3,8-diaza-bicyclo[4.2.0]octane and 2-[1,2,3]triazol-2-yl-benzoic acid (Intermediate 14) for 2-thiophen-2-yl-benzoic acid. DCM was used in place of DMF. MS (ESI) mass calcd. For C22H19ClN6O2, 434.89; m/z found 435.1 [M+H]+. 1H NMR (CD3OD): 8.03-7.28 (m, 6H), 7.23-6.88 (m, 3H), 4.72-4.54 (m, 1H), 4.35-3.96 (m, 3H), 3.90-3.35 (m, 3H), 3.13-1.71 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680275B2
Source datasetuspto-grants-2014_03
ORD IDord-036eb463caad4f3280000b868be6146c
Source noteuspto-grants-2014_03