Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378437Generated: October 30, 2026

Triethylamine → 2,1,3-Benzoxadiazol-5-amine

https://huagongshe.com/reaction/2378437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2,1,3-Benzoxadiazole-5-carboxylic acidHCID 2735454—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2,1,3-Benzoxadiazol-5-amineHCID 430696441%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a solution of 2,1,3-benzoxadiazole-5-carboxylic acid (102 mg, 0.621 mmol) in THF (3 mL) was added triethylamine (103 μL, 0.739 mmol) followed by DPPA (160 μL, 0.739 mmol) at room temperature. The mixture was stirred for 4 h, diluted with CH2Cl2 and washed with water. The organic layer was dried over MgSO4, concentrated and purified by flash chromatography on silica gel with 0 to 50% EtOAc in CH2Cl2. The resulting material was dissolved in AcOH (2 mL) and water (0.7 mL) was added dropwise yielding a slightly cloudy solution which was heated at 105° C. for 30 min. The mixture was cooled, made basic with sat. Na2CO3 solution and extracted several times with THF. The combined organic layers were dried over MgSO4, concentrated and purified by flash chromatography on silica gel eluting with 0 to 15% MeOH in CH2Cl2 to give 34 mg (41%) of compound 480A as a yellow solid. HPLC: 100% at 1.27 min (retention time) (YMC S5 ODS column, 4.6×50 mm Ballistic, 10-90% aqueous methanol over 4 mincontaining 0.2% H3PO4, 4 mL/min, monitoring at 220 nm). MS (ES): m/z 136.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470797B2
Source datasetuspto-grants-2008_12
ORD IDord-d17f7a5f32da446d8d7ce0089141b0d1
Source noteuspto-grants-2008_12