HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → (5-Chloromethyl-quinolin-2-yl)-(5-methyl-furan-2-ylmethyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | {2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinolin-5-yl}-methanol | HCID 44218152 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Chloromethyl-quinolin-2-yl)-(5-methyl-furan-2-ylmethyl)-amine | HCID 68436366 | — |
Reaction Steps
{2-[(5-Methyl-furan-2-ylmethyl)-amino]-quinolin-5-yl}-methanol (example 41, step A, 70 mg, 0.261 mmol) was dissolved in 2 mL tetrahydrofurane and methanesulfonyl chloride (34 mg, 0.297 mmol) and N,N-diisopropyl ethyl amine (41 mg, 0.318 mmol) were added. The reaction mixture was stirred at room temperature overnight and the solvent was evaporated off. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 100:0->50:50 gradient). (5-Chloromethyl-quinolin-2-yl)-(5-methyl-furan-2-ylmethyl)-amine was obtained as a brown solid (59 mg, 79%), MS: m/e=287.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07825253B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-e2cac7a370c34b74b95a55a09558e1dd |
| Source note | uspto-grants-2010_11 |