HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 178495798, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(2-Methoxy-ethyl)-4,5-dimethyl-3H-thiazol-2-ylideneamine | HCID 66851723 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178495798 | HCID 178495798 | 35% |
Reaction Steps
The product of Example 126A (0.20 g, 1.1 mmol), Et3N (0.45 mL, 3.2 mmol) and benzoyl chloride (Aldrich, 0.16 mL, 1.4 mmol) in 15 mL THF were processed using the method described in Example 129 to afford the title compound (0.11 g, 0.38 mmol, 35% yield). 1H NMR (300 MHz, CDCl3) δ ppm 2.24 (s, 3H), 2.27 (d, J=0.7 Hz, 3H), 3.32 (s, 3H), 3.82 (t, J=5.3 Hz, 2H), 4.41 (t, J=5.3 Hz, 2H), 7.38-7.51 (m, 3H), 8.27-8.34 (m, 2H); MS (DCI/NH3) m/z291 (M+H)+; Anal. calculated for C15H18N2O2S: C, 62.04; H, 6.25; N, 9.65. Found: C, 62.02; H, 6.05; N, 9.56.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546583B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-dd812402d1a64211b2e77b6324e223fe |
| Source note | uspto-grants-2013_10 |