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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-butyl (2-(7-oxo-7-((pyridin-3-ylmethyl)amino)heptanamido)phenyl)carbamate | HCID 90398241 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N1-(2-aminophenyl)-N7-(pyridin-3-ylmethyl)heptanediamide | HCID 78322689 | 64.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133105B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-753fac27aac94eb2b79eb9cbb9968542 |
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| Source note | uspto-grants-2015_09 |
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