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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869705Generated: October 30, 2026

N-[(2R)-1-(4-Methoxy-3-sulfamoylphenyl)propan-2-yl]acetamide → 5-(2-Aminopropyl)-2-methoxybenzene-1-sulfonamide

https://huagongshe.com/reaction/1869705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[(2R)-1-(4-Methoxy-3-sulfamoylphenyl)propan-2-yl]acetamideHCID 14099978—
SolventHydrochloric AcidHCID 313—
Product5-(2-Aminopropyl)-2-methoxybenzene-1-sulfonamideHCID 10060387—

Reaction Steps

Intermediate XI (10.5 g) is boiled in 5% HCl (250 ml) under a reflux condenser for 16 to 18 h. The course of the reaction is controlled with TLC detecting the starting substance. After the reaction is complete, the reaction mixture is concentrated to about ⅓ of its volume, then, a saturated solution of sodium carbonate (50 ml) is slowly added dropwise under stirring. After the addition, pH˜10 is controlled and the reaction mixture is stirred for 0.5 hour, then let to crystallize at 0° C. The precipitated crystals are sucked off and the filtrate is concentrated to ½ of its volume and let to crystallize at 0° C. Both fractions (4 g+8 g) of white to brownish crystals are combined and re-crystallized from water. The yield is 7.52 g (80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638649B2
Source datasetuspto-grants-2009_12
ORD IDord-92c917812a0e45359dd9ff783f790032
Source noteuspto-grants-2009_12