HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-C]pyridine → {(S)-6-[(R)-4-(2-Methyl-2,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-ylmethyl)-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-C]pyridine | HCID 15908773 | — |
| Reactant | {(S)-6-[(R)-4-Bromomethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester | HCID 86700813 | — |
| Product | {(S)-6-[(R)-4-(2-Methyl-2,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-ylmethyl)-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester | HCID 90313806 | — |
Reaction Steps
The title compound is prepared from {(S)-6-[(R)-4-bromomethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester and 2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridine following a procedure analogous to that described for Intermediate 42. LC (method 1): tR=0.92 min; Mass spectrum (ESI+): m/z=542 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927531B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-6ea8fca482a34274b22f4c00fa0af9c4 |
| Source note | uspto-grants-2015_01 |