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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354882Generated: October 31, 2026

Sodium Hydroxide → HCID 45487115, compound

https://huagongshe.com/reaction/2354882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 16045395HCID 16045395—
SolventTetrahydrofuranHCID 8028—
ProductHCID 45487115HCID 45487115—

Reaction Steps

Sodium hydroxide (0.5 mL, 3 N solution) was added to a solution 12-(4-chloro-benzenesulfonyl)-4,5,12-triaza-tricyclo[6.3.1.02,6]dodeca-2(6),3-diene-10-carboxylic acid ethyl ester (321 mg, 0.783 mmol) in THF (2 mL). The resulting mixture was stirred at room temperature for 4 h. The reaction mixture was extracted with EtOAc (2×5 mL) and the combined organic phases were dried (Na2SO4), filtered, concentrated and purified by preparative HPLC to give 12-(4-chloro-benzenesulfonyl)-4,5,12-triaza-tricyclo[6.3.1.02,6]dodeca-2(6),3-diene-10-carboxylic acid as a white solid. Retention time (min)=1.316, method [1], MS (ESI) 382.0 (M+H); 1H NMR (300 MHz, CDCl3) δ 7.56 (d, J=8.7 Hz, 2H), 7.30-7.22 (m, 3H), 5.30-5.25 (m, 1H), 4.54-4.45 (m, 1H), 2.80 (dd, J=17.0, J=7.7 Hz, 1H), 2.50 (d, J=17.0 Hz, 1H), 2.42-2.30 (m, 1H), 2.24-1.85 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754712B2
Source datasetuspto-grants-2010_07
ORD IDord-e8ac724cd72a4d6ab28543597cb48cc1
Source noteuspto-grants-2010_07