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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256168Generated: November 1, 2026

HCID 86655238, compound → HCID 67310994, compound

https://huagongshe.com/reaction/1256168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86655238HCID 86655238—
SolventAmmoniumHCID 223—
SolventMethanolHCID 887—
ProductHCID 67310994HCID 6731099437.5%

Reaction Steps

A solution of 2,2,2-trifluoro-N-(4-(N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)sulfamoyl)-3-((5-methyl-1,3,4-oxadiazol-2-yl)methyl)phenyl)acetamide (300 mg, 0.60 mmol) in 7M ammonium in MeOH (10 mL) was stirred in a sealed tube at 50° C. for 16 hours. After concentrated, the crude mixture was purified by prep HPLC (SunFire Prep C18 OBD 5 uM 30×50 mm column) to give the title compound as a yellow solid (90 mg, yield 37%). MS calcd for (C14H17BN4O5S): 400.2. MS found (ESI negative): (M−H)−=399.1. 1H NMR (DMSO-d6) δ (ppm): 10.0 (s, 1H), 9.20 (bs, 1H), 7.56 (d, J=8.8 Hz, 1H), 7.42 (s, 1H), 7.22 (d, J=8.4 Hz, 1H), 7.11 (d, J=8.4 Hz, 1H), 6.41 (d, J=8.4 Hz, 1H), 6.26 (s, 1H), 4.85 (s, 2H), 4.41 (s, 2H), 2.39 (s, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-f38233a5ca1b433ba7fb433e7ada990c
Source noteuspto-grants-2013_06