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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256117Generated: November 1, 2026

Ethylamine → HCID 67312270, compound

https://huagongshe.com/reaction/1256117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantTriethylamineHCID 8471—
ReactantPyBOPHCID 2724699—
ReactantHCID 53234452HCID 53234452—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 67312270HCID 67312270—

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 ethyl amine (2.1 mg, 4.2 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 (C17H20BN3O5S): 389.12. MS found (ESI negative): (M−H)−=388.1. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.86 (s, 1H), 9.15 (br, 1H), 7.98 (m, 1H), 7.41 (s, 1H), 7.39 (d, J=8.8 Hz, 1H), 7.21 (d, J=8 Hz, 1H), 7.09 (dd, J=8.4 Hz, 1H), 6.44 (d, J=2 Hz, 1H), 6.33 (dd, J=8.8 Hz, 1H), 4.85 (s, 2H), 3.75 (s, 2H), 3.09 (m, 1H), 1.02 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-0dcacb05888846b88c1acc05b9e66c2c
Source noteuspto-grants-2013_06