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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256115Generated: October 26, 2026

Azane;hydrate → 2-(5-Amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)acetamide

https://huagongshe.com/reaction/1256115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzane;hydrateHCID 12896473—
ReactantMethyl 2-(2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)-5-(2,2,2-trifluoroacetamido)phenyl)acetateHCID 86655206—
SolventMethanolHCID 887—
Product2-(5-Amino-2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)phenyl)acetamideHCID 53234457—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of methyl 2-(2-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)-5-(2,2,2-trifluoroacetamido)phenyl)acetate (0.5 g, 0.001 mol) and aq. NH3.H2O (28%, 10 mL) in CH3OH was stirred at 50° C. over night. The mixture was concentrated and the residue dissolved in ethyl acetate and washed with brine, dried and concentrated, purified by column chromatography (PE:EA 5:1˜1:3) to give the title compound, which was dissolved in MeCN, acidified with aq. HCl and freeze-dried to give the product as hydrochloride salt (200 mg, yield 53%). 1HNMR DMSO-d6 400 MH. δ9.85 (s, 1H), 9.17 (s, 1H), 7.43-6.32 (m, 6H), 5.92 (s, 2H), 4.86 (s, 2H), 3.74 (s, 2H). LC-MS m/z 360 (M−H, negative); HPLC purity: 96.93% (220 nm), 99.27% (254 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-273667dedd1348bca67f8d4c3ac9fb07
Source noteuspto-grants-2013_06