Table 1. Insecticidal activities of 6-phenoxy quinoline derivatives against Plutella xylostella, Spodoptera litura, and Frankliniella occidentalis.
| ||||||||
|---|---|---|---|---|---|---|---|---|
| Compound No. (1st screening) | R1 | R2 | R3 | R4 | R5 | EC90 (mg a.i./L) | ||
| P. xylosotella | S. litura | F. occidentalis | ||||||
| cpd1 (Lead) | Me | Me | Cl | H | 4′-Cl | 100 | >100 | >200 |
| cpd8 | Et | Me | Cl | H | 4′-Cl | 5–20 | >100 | 50–200 |
| cpd9 | n-Bu | Me | Cl | H | 4′-Cl | >100 | >100 | >200 |
| cpd10 | Me | OMe | Cl | H | 4′-Cl | 10–20 | >100 | >200 |
| cpd11 | Me | t-Bu | Cl | H | 4′-Cl | >100 | >100 | >200 |
| cpd12 | Me | Me | CF3 | H | 4′-Cl | <20 | 100 | 200 |
| cpd13 | Me | Me | CN | H | 4′-Cl | >100 | >100 | >200 |
| cpd14 | Me | Me | Me | H | 4′-Cl | 20–100 | >100 | >200 |
| cpd15 | Me | Me | Cl | H | 2′-Cl | 100 | >100 | >200 |
| cpd16 | Me | Me | Cl | H | 3′-Cl | 20–100 | >100 | >200 |
| cpd17 | Me | Me | Cl | H | 4′-CN | 100 | 20–100 | >200 |
| cpd18 | Me | Me | Cl | H | 4′-Me | >100 | >100 | N.D. |
| cpd19 | Me | Me | Cl | H | 4′-F | 100 | >100 | >200 |
| cpd20 | Me | Me | Cl | H | 4′-CF3 | 20–100 | 20–100 | <50 |
| cpd21 | Me | Me | Cl | H | 4′-OMe | >100 | >100 | >200 |
| cpd22 | Me | Me | Cl | H | 4′-OCF3 | <20 | 100 | <50 |
| cpd23 | Me | Me | CF3 | H | 4′-OCF3 | 1.25–2.5 | 2.5–5 | 20–50 |
| cpd24 | Me | Me | Me | H | 4′-OCF3 | 20–100 | 20–100 | 100–200 |
| cpd25 | Me | Me | H | Me | 4′-OCF3 | 2.5–5 | 20–100 | 100–200 |
| cpd26 | Me | Me | Me | Me | 4′-OCF3 | 5–20 | 20–100 | 100 |
| cpd27 | Me | Me | Cl | Cl | 4′-OCF3 | >100 | >100 | 20–100 |
N.D.: No Data, mg a.i./L: mg active ingredient/L