HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Pyridinemethanamine → HCID 178419300, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Pyridinemethanamine | HCID 31018 | — |
| Reactant | HCID 12535780 | HCID 12535780 | — |
| Reactant | Methylenechloride Hexane | HCID 21226440 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | HCID 178419300 | HCID 178419300 | 61% |
Reaction Steps
A solution of 0.4 g (1.3 mmol) of 8-bromo-5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-thione (Sahni, S., et al., J. Indian Chem. Soc., 56:625 (1979)) in 10 mL of 2-ethoxyethanol was treated with 0.28 mL (2.1 mmol) of 3-(aminomethyl)-pyridine and heated at reflux overnight. The solvent was removed under reduced pressure and the residue taken up in EtOAc and washed three times with H2O, then saturated NaHCO3 solution and saturated NaCl solution. Drying over MgSO4 and removal of the solvent under reduced pressure left the crude product. Trituration with CH2Cl2 /hexane, then with Et2O/hexane left 0.3 g (61% yield) of the product as a yellow solid, mp 152-155° C. The structure was confirmed by NMR and mass spectroscopy. (m+H)+ =379.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919780 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-73bc8ce7c28948359cfb12c9380d8420 |
| Source note | uspto-grants-1999_07 |