HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Carbamate → HCID 86609398, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Carbamate | HCID 11722 | — |
| Reactant | HCID 50994269 | HCID 50994269 | — |
| Reactant | HCID 86609399 | HCID 86609399 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 86609398 | HCID 86609398 | — |
Reaction Steps
(2-Chloro-pyridin-4-yl)-(3,5-dibromo-phenyl)-methanone was converted to [3-bromo-5-(2-chloro-pyridine-4-carbonyl)-phenyl]-carbamic acid methyl ester under the palladium catalyzed conditions described for Example 86, using carbamic acid methyl ester in place of methanesulfonamide. The Suzuki reaction and removal of the triisopropylsilyl protecting group were carried out as described in Example 35. 1H NMR (400 MHz, CDCl3): δ 8.56 (d, J=4.9 Hz, 1H), 8.35 (s, 1H), 8.07 (s, 1H), 7.82 (s, 1H), 7.77 (t, J=1.5 Hz, 1H), 7.69 (s, 1H), 7.55 (dd, J=5.0, 1.3 Hz, 1H), 7.43 (d, J=8.2 Hz, 1H), 7.30-7.25 (m, 2H), 7.18 (dd, J=7.2, 0.8 Hz, 1H), 6.85 (s, 1H), 6.71 (s, 1H), 3.81 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504401B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-36127330c5584e7fa7702fe68790e3b4 |
| Source note | uspto-grants-2009_03 |