HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 3-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]-N-methylbutanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]butanoic acid | HCID 68431618 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]-N-methylbutanamide | HCID 68432459 | 74% |
Reaction Steps
Oxalylchloride (2 mL, 3.9 mmol) was added during 5 minutes to 3-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]butanoic acid in DCM (40 mL) and DMF (5 drops) under argon. The mixture was stirred at r.t. for 3 h and then was MeNH2 (2M in THF, 3.6 mL, 7.2 mmol) added and the resulting mixture was stirred o.n. Saturated NaHCO3 (75 mL) was added and the mixture was extracted with CHCl3 (3×100 mL). The combined organic phases were dried (MgSO4) and concentrated. The crude was purified by flash column chromatography (SiO2, Heptane-EtOAc 1:2) to give 0.74 g (74%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691892B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-714cd48aca3f4814868601b71f9ed54c |
| Source note | uspto-grants-2010_04 |