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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035822Generated: October 26, 2026

Water → HCID 178505020, compound

https://huagongshe.com/reaction/1035822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantN-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)methanesulfonamideHCID 71060214—
SolventDimethylformamideHCID 6228—
ProductHCID 178505020HCID 17850502090%

Reaction Conditions

Temperature120 °C

Reaction Steps

N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)methanesulfonamide 7 (0.12 g, 0.338 mmol) was dissolved in anhydrous DMF (10 mL), Sodium azide (0.088 g, 1.35 mmol) and ammonium chloride (0.072 g, 1.35 mmol) were added to above solution. Resulting suspension was heated at 120° C. for overnight (14 hours). Reaction was cooled down and water was added. Resulting (precipitated) solid was filtered, washed with water, methanol, and water. This was further purified by dissolving into DMSO and re-precipitated with addition of water. Resulting solid was filtered, washed with water, methanol and dried under high vacuum to yield N-(3-((5-(4-(1H-tetrazol-5-yl)phenyl)oxazol-2-yl)amino)phenyl)methanesulfonamide 41 (0.12 g, 90%) as a white solid. MS (ES) m/z 398 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546400B2
Source datasetuspto-grants-2013_10
ORD IDord-5486a5a32b2a4cbaa751ac313b3fd253
Source noteuspto-grants-2013_10