HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boronic Acid → tert-Butyl (5-bromo-4-cyclopropyl-1,3-thiazol-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | HCID 57634141 | HCID 57634141 | — |
| Reactant | HCID 86635458 | HCID 86635458 | — |
| Product | tert-Butyl (5-bromo-4-cyclopropyl-1,3-thiazol-2-yl)carbamate | HCID 45117858 | — |
| Product | HCID 57634141 | HCID 57634141 | — |
Reaction Steps
Example 170, N—((S)-2-amino-3-(6-trifluoromethyl)pyridine-3-yl)propyl)-5-(isoquinolin-6-yl)thiazol-2-amine: The title compound was synthesized in a manner similar to that described for Example 81 using (S)-tert-butyl 1-(5-bromothiazol-2-yl-(Boc)-amino)-3-(6-(trifluoromethyl)pyridin-3-yl)propan-2-ylcarbamate to couple with the boronic acid. (S)-tert-butyl 1-(5-bromothiazol-2-yl-(Boc)-amino)-3-(6-(trifluoromethyl)pyridin-3-yl)propan-2-ylcarbamate was synthesized as shown in Scheme 39. Theoretical (M+H) 430.4 found 430.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084479B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-5e4915fb0d454881b8486f5e9355e377 |
| Source note | uspto-grants-2011_12 |