HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioacetamide → (1S)-1-(1-{[2-cyano-4-(2-methyl-1,3-thiazol-4-yl)quinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1-(trifluoromethyl)propyl 4-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | (S)-1-(1-{[4-(bromoacetyl)-2-cyanoquinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1-(trifluoromethyl)propyl 4-nitrobenzoate | HCID 86621977 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (1S)-1-(1-{[2-cyano-4-(2-methyl-1,3-thiazol-4-yl)quinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1-(trifluoromethyl)propyl 4-nitrobenzoate | HCID 66791140 | — |
Reaction Steps
A solution of 1-(1-{[4-(bromoacetyl)-2-cyanoquinolin-7-yl]methyl}-1H-1,2,3-triazol-4-yl)-1-(trifluoromethyl)propyl 4-nitrobenzoate (see Example 52, Step 2) (65 mg, 0.1 mmol) and thioacetamide (9 mg, 0.11 mmol) in DMF (1 mL) was stirred at 100° C. overnight. The reaction mixture was diluted in ethyl acetate, washed with water, brine and dried over MgSO4. The crude compound was purified on silica gel (eluting solvent: 3% acetone in dichloromethane) to give the desired product. 1H NMR (acetone-d6): δ 8.85 (d, 1H), 8.52 (s, 1H), 8.42 (d, 2H), 8.30 (d, 2H), 8.17 (d, 2H), 8.05 (s, 1H), 7.75 (d, 1H), 6.05 (s, 2H), 3.05 (m, 1H), 2.85 (s, 3H), 2.85 (m, 1H), 1.15 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960409B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-b12510f493154f9f832746649fa0c80d |
| Source note | uspto-grants-2011_06 |