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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714179Generated: November 4, 2026

Ammonium Chloride → tert-Butyl {3-[6-amino-1-(3-methylbut-2-enyl)-1H-benzimidazol-2-ylsulfanyl]propyl}carbamate

https://huagongshe.com/reaction/1714179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-butyl {3-[1-(3-methylbut-2-enyl)-6-nitro-1H-benzimidazol-2-ylsulfanyl]propyl}carbamateHCID 86619700—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Producttert-Butyl {3-[6-amino-1-(3-methylbut-2-enyl)-1H-benzimidazol-2-ylsulfanyl]propyl}carbamateHCID 59464722107.1%

Reaction Steps

A solution of 140 mg (0.33 mmol) of tert-butyl {3-[1-(3-methylbut-2-enyl)-6-nitro-1H-benzimidazol-2-ylsulfanyl]propyl}carbamate in 15 ml of ethanol was added dropwise to a suspension of 93 mg (1.66 mmol) of iron and 16 mg (0.30 mmol) of ammonium chloride in 1.5 ml of water and boiled at reflux for 3 hours. The catalyst was filtered off and washed with ethanol. The filtrate was concentrated under reduced pressure. The 138 mg of the desired product thus obtained were used in the next stage without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795445B2
Source datasetuspto-grants-2010_09
ORD IDord-bf785caf84134e6c8724c8b7052e787f
Source noteuspto-grants-2010_09