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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276698Generated: November 1, 2026

Hydrochloric Acid → N1-(2-aminophenyl)-N7-(pyridin-3-ylmethyl)heptanediamide

https://huagongshe.com/reaction/2276698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-butyl (2-(7-oxo-7-((pyridin-3-ylmethyl)amino)heptanamido)phenyl)carbamateHCID 90398241—
SolventEthyl AcetateHCID 8857—
ProductN1-(2-aminophenyl)-N7-(pyridin-3-ylmethyl)heptanediamideHCID 7832268964.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a solution of tert-butyl (2-(7-oxo-7-((pyridin-3-ylmethyl)amino)heptanamido)phenyl)carbamate (1.2 g, 2.73 mmol) in EtOAc (50 mL) were passed HCl (gas) at 0° C. The mixture was stirred for 30 min at 0° C. under HCl (gas). A white solid precipitated and was filtered. The white solid was collected and poured into a solution of 5% Na2CO3 in water (100 mL). The resulting mixture was extracted by EtOAc (100 mL×2). The organic layers were combined, dried with anhydrous Na2SO4 and concentrated under reduce pressure. The crude solid was recrystallized in EtOAc to afford the desired compound (0.6 g, yield 64.6%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133105B2
Source datasetuspto-grants-2015_09
ORD IDord-753fac27aac94eb2b79eb9cbb9968542
Source noteuspto-grants-2015_09