HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Acetate → 2,6-Diethoxy-3'-fluoro-4'-morpholin-4-ylmethyl-biphenyl-4-ylmethy-pyrimidine-2,4-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | 4-(4-Bromo-2-fluorobenzyl)morpholine | HCID 21914503 | — |
| Reactant | 5-(3,5-Diethoxy-4-iodo-benzyl)-pyrimidine-2,4-diamine | HCID 22636919 | — |
| Reactant | 5-(2,6-Diethoxy-3'-fluoro-4'-morpholin-4-ylmethyl-biphenyl-4-ylmethyl)-pyrimidine-2,4-diamine | HCID 22636960 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | 2,6-Diethoxy-3'-fluoro-4'-morpholin-4-ylmethyl-biphenyl-4-ylmethy-pyrimidine-2,4-diamine | HCID 136388389 | — |
Reaction Steps
Analogously to example (4a), starting from 4-(4-bromo-2-fluoro-benzyl)-morpholine (274 mg; 1 mmol), bis(pinacolato)diboron (380 mg; 1.5 mmol), potassium acetate (294 mg; 3 mmol), bis(triphenylphosphine)palladium(II) dichloride (47 mg; 0.07 mmol) and from 5-(3,5-diethoxy-4-iodo-benzyl)-pyrimidine-2,4-diamine (example 1) (248 mg; 0.6 mmol), 166 mg (34%) 5-(2,6-diethoxy-3′-fluoro-4′-morpholin-4-ylmethyl-biphenyl-4-ylmethyl)-pyrimidine-2,4-diamine are obtained as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06821980B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-258c51d9e3ad4e469eb720c55ba17d25 |
| Source note | uspto-grants-2004_11 |