HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-6-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol → HCID 86692934, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-6-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol | HCID 17750230 | — |
| Reactant | HCID 66715820 | HCID 66715820 | — |
| Product | HCID 86692934 | HCID 86692934 | 71.4% |
Reaction Steps
Following general procedure D, 1-{6-bromo-4-[4-(pyrrolidin-1-ylmethyl)piperidin-1-yl]quinolin-3-yl}ethanone (30 mg, 0.072 mmol) was reacted with 2-chloro-6-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (43 mg, 0.150 mmol) to afford the desired product (25.4 mg, 71%) as a yellow brown solid: 1H NMR (500 MHz, CD3OD) δ 8.80 (s, 1H), 8.29 (s, 1H), 8.03 (s, 2H), 7.30 (d, J=2.1 Hz, 1H), 7.24 (d, J=2.0 Hz, 1H), 3.99 (s, 3H), 3.49 (d, J=12.9 Hz, 2H), 3.24-3.12 (m, 6H), 3.02 (d, J=5.5 Hz, 2H), 2.70 (s, 3H), 2.13-1.96 (m, 7H), 1.77-1.62 (m, 2H); ESI MS m/z 494 [C28H32ClN3O3+H]+; HPLC>99% (AUC), tR=10.45 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-99ac654ce644483a93303a0f390bd909 |
| Source note | uspto-grants-2015_09 |