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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256122Generated: October 31, 2026

Isobutylamine → HCID 67310372, compound

https://huagongshe.com/reaction/1256122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
ReactantPyBOPHCID 2724699—
ReactantHCID 53234452HCID 53234452—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67310372HCID 6731037251.5%

Reaction Steps

To a stirred solution of 2-(5-amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)acetic acid (720 mg, 2 mmol) and isobutylamine (1.2 mL, 12 mmol) in 20 mL of DMF was added PyBOP (1550 mg, 3 mmol) and TEA (1 mL, 7 mmol). The reaction mixture was stirred for 16 hours. After water was added, the reaction mixture was extracted with ethyl acetate and washed with water, 1N HCl and brine. The organic layer was dried over Na2SO4 and concentrated. The crude residue was purified by ISCO CombiFlash Rf silica chromatography eluted with 88:10:2 chloroform:MeOH:H2O to give the desired product as a yellow solid (430 mg, yield 51%). MS calcd for (C19H24BN3O5S): 417.2. MS found (ESI negative): (M−H)−=416.1. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.89 (s, 1H), 9.17 (bs, 1H), 7.96 (t, J=5.6 Hz, 1H), 7.41 (m, 2H), 7.22 (d, J=8.4 Hz, 1H), 7.10 (d, J=8 Hz, 1H), 6.47 (s, 1H), 6.34 (d, J=8 Hz, 1H), 5.93 (bs, 2H), 4.87 (s, 2H), 3.80 (s, 2H), 2.93 (t, J=6.4 Hz 2H), 1.72 (m, 1H), 0.85 (d, J=7.8 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-0a4da9800cba405ba22b37e804b24d17
Source noteuspto-grants-2013_06