HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34919Generated: October 25, 2026
Ammonium Hydroxide → HCID 19851782, compound
https://huagongshe.com/reaction/34919
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-[4-(5-Bromo-3-methylpyrid-2-yl)butyl]-6-(pyrid-3-ylmethyl)-3H-1,2,3-Triazolo[5,4-b]pyridine | HCID 19851773 | — |
| Product | HCID 19851782 | HCID 19851782 | — |
Reaction Steps
A mixture of 3-[4-(5-bromo-3-methylpyrid-2-yl)butyl]-6-(pyrid-3-ylmethyl)3H-1,2,3-triazolo[5,4-b]-pyridine (3.9 g) and polyphosphoric acid (ca. 35 g) was heated with stirring at 190°-200° C. for 40 minutes. The cooled residue was dissolved in aqueous ammonium hydroxide to give a solution of ca. pH 8 and extracted with chloroform (4×100 ml). The combined chloroform extracts were dried over magnesium sulphate, concentrated in vacuo to yield 0.6 g title compound (h) m.p. 162°-5° C. The aqueous fraction was evaporated to dryness to yield a pasty residue, which gave on extraction with hot chloroform a further 0.25 g (h) m.p. 163°-164° C. on evaporation. The residue was then heated under reflux with chloroform for 2 hr. and the chloroform solution was chromatographed on silica gel to yield 1.02 g title compound (i) m.p. 110°-112° c.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04764519 |
|---|
| Source dataset | uspto-grants-1988_08 |
|---|
| ORD ID | ord-c374d1e86f8e4e73aa6d4ea1a1c7d07e |
|---|
| Source note | uspto-grants-1988_08 |
|---|