HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannane, tributyl(1-methylethenyl)- → HCID 68973673, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannane, tributyl(1-methylethenyl)- | HCID 10871254 | — |
| Reactant | HCID 68972631 | HCID 68972631 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 68973673 | HCID 68973673 | — |
Reaction Steps
3-(5-Bromo-thiophen-2-yl)-2(S)-{[6-(4-tert-butyl-phenoxy)-1-cyclopentylmethyl-isoquinoline-3-carbonyl]-amino}-propionic acid methyl ester (prepared in Example 38) was treated with tributyl-isopropenyl-stannane and Pd(PPh3)4 as described in the general procedure M to afford 2(S)-{[6-(4-tert-butyl-phenoxy)-1-cyclopentylmethyl-isoquinoline-3-carbonyl]-amino}-3-(5-isopropenyl-thiophen-2-yl)-propionic acid methyl ester. This was treated with Pd/C and H2 (1 atm) by the general procedure N to afford 2(S)-{[6-(4-tert-butyl-phenoxy)-1-cyclopentylmethyl-isoquinoline-3-carbonyl]-amino}-3-(5-isopropyl-thiophen-2-yl)-propionic acid methyl ester. This ester was hydrolyzed by the general procedure C to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208601B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-0c516c659fa04a99b51f30105677e697 |
| Source note | uspto-grants-2007_04 |