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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441127Generated: October 29, 2026

Hydrazine hydrate (1:1) → N-(5-aminoacetylamino-4-nitro-2-phenoxyphenyl)methanesulfonamide

https://huagongshe.com/reaction/441127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-(4-nitro-2-phenoxy-5-phthalimidoacetylaminophenyl)methanesulfonamideHCID 22406108—
SolventDichloromethane methanolHCID 21226129—
ProductN-(5-aminoacetylamino-4-nitro-2-phenoxyphenyl)methanesulfonamideHCID 2240611073.5%

Reaction Steps

To 350 ml of a dichloromethane-methanol (5:2) solution containing 9.5 g of N-(4-nitro-2-phenoxy-5-phthalimidoacetylaminophenyl)methanesulfonamide was added 0.64 ml of 99% hydrazine monohydrate at room temperature, followed by stirring for 19 hours. The precipitate was removed by filtration, followed by washing with hot acetonitrile. The filtrate was washed with water, and concentrated under reduced pressere. The resulting precipitate was washed with ethanol and dried to give 5.2 g of N-(5-aminoacetylamino-4-nitro-2 -phenoxyphenyl)methanesulfonamide as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521311
Source datasetuspto-grants-1996_05
ORD IDord-a8948d2e22914161856ac9ca49e3a941
Source noteuspto-grants-1996_05