HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borate(1-), trifluoro(1-piperidinylmethyl)-, potassium (1:1), (T-4)- → {(S)-6-[(R)-4-Piperidin-1-ylmethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borate(1-), trifluoro(1-piperidinylmethyl)-, potassium (1:1), (T-4)- | HCID 23706007 | — |
| Reactant | {(S)-6-[(R)-4-bromo-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester | HCID 86700774 | — |
| Product | {(S)-6-[(R)-4-Piperidin-1-ylmethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester | HCID 90313304 | — |
Reaction Steps
The title compound is prepared from {(S)-6-[(R)-4-bromo-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester and potassium piperidin-1-ylmethyltrifluoroborate following a procedure analogous to that described for Intermediate 3. LC (method 5): tR=1.15 min; Mass spectrum (ESI+): m/z=490 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927531B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-38c2b61566164b21939b49753ca9ef73 |
| Source note | uspto-grants-2015_01 |