HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702324Generated: October 29, 2026
3-Pyridinemethanamine → HCID 15961237, compound
https://huagongshe.com/reaction/1702324
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Pyridinemethanamine | HCID 31018 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | 3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amine | HCID 10220561 | — |
| Reactant | 3,4-Dimethoxy-1,2,5-thiadiazole 1-oxide | HCID 12913947 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15961237 | HCID 15961237 | — |
Reaction Steps
A solution of 3-(3-piperidinomethylphenoxy)propylamine (from the dihydrochloride, 3.21 g; 10.0 mmoles) in 30 ml of methanol was added dropwise over a period of 60 minutes to a partial solution of 3,4-dimethoxy-1,2,5-thiadiazole 1-oxide (1.62 g; 10.0 mmoles) that had been cooled to 5°-7° in an ice-water bath. After 3 hours at ambient temperature, a solution of 3-aminomethylpyridine (1.14 g; 10.5 mmoles) in 10 ml of methanol was added and the solution was then stirred for 18 hours. The reaction mixture was evaporated under reduced pressure and the residue chromatographed by flash chromatography on 100 g of silica gel (230-400 mesh) using methylene chloride-methanol-ammonia. The appropriate fractions were combined, evaporated and triturated with acetonitrile to give 4.05 g of product. Recrystallization from isopropyl alcohol yielded the title compound, mp 139.5°-143°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04380638 |
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| Source dataset | uspto-grants-1983_04 |
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| ORD ID | ord-cb486a19839d4efe8b593d6956a11b87 |
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| Source note | uspto-grants-1983_04 |
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