HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[1-(diphenylmethyl)-3-azetidinyl]methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-Amino-1-(diphenylmethyl)azetidine | HCID 5744546 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[1-(diphenylmethyl)-3-azetidinyl]methanesulfonamide | HCID 57436107 | — |
Reaction Steps
A solution of 1-(diphenylmethyl)-3-azetidinamine (synthesized according to the methods of Arimoto et. al., J. of Antibiotics 39 (9), 1243-56, 1986) (197 mg, 0.83 mmol) in dichloromethane (10 mL) was treated with excess triethylamine at 0° C. followed by methanesulfonyl chloride (71 μL, 0.91 mmol). The reaction was stirred for 30 minutes and then concentrated and purified on silica gel (0-10% methanol/dichloromethane) to provide 185 mg of the desired product as a white solid. LC/MS: M+H 317.19 at 0.31 minutes, Method D.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07625909B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-27c8f06d388a4846b3fa8011d40fd0c3 |
| Source note | uspto-grants-2009_12 |