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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256123Generated: November 1, 2026

Triethylamine → HCID 67310574, compound

https://huagongshe.com/reaction/1256123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclopropylamineHCID 69828—
ReactantPyBOPHCID 2724699—
ReactantHCID 53234452HCID 53234452—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 67310574HCID 67310574—

Reaction Steps

To the mixture of 2-(5-amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)acetic acid (500 mg, 1.4 mmol) and cyclopropyl amine (0.5 ml, 7 mmol) in DMF (5 ml), added PyBOP (730 mg, 1.4 mmol) then triethyl amine (0.4 ml, 3 mmol). Stirring was kept for 3 hours. Diluted with EtOAc, washed with 1N HCl, water and brine. Dried over anhydrous sodium sulfate. Concentrated, the residue was dissolved in DMSO and purified by prep HPLC (SunFire Prep C18 OBD 5 uM 30×50 mm column). The title compound was obtained as white powder. MS calcd for (C18H20BN3O5S): 401.12. MS found (ESI negative): (M−H)−=400.1. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.84 (s, 1H), 8.14 (d, J=4 Hz, 1H), 7.43 (s, 1H), 7.42 (d, J=8.8 Hz, 1H), 7.24 (d, J=8.4 Hz, 1H), 7.11 (dd, J=8.4 Hz, 1H), 6.43 (d, J=2 Hz, 1H), 6.36 (dd, J=8.4 Hz, 1H), 4.88 (s, 2H), 3.74 (s, 2H), 2.67 (m, 1H), 0.64 (m, 2H), 0.44 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-71c5d39b37e144b5999057f307735046
Source noteuspto-grants-2013_06