HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzyl chloride → {(R)-7-[5-(4-Fluoro-benzyl)-[1,2,3]triazol-1-yl]-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl}-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | Azide | HCID 33558 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 1-Fluoro-4-prop-2-ynyl-benzene | HCID 10558668 | — |
| Reactant | {7-[5-(1-Phenyl-cyclopentyl)-[1,2,3]triazol-1-yl]-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl}-acetic acid | HCID 46893926 | — |
| Product | {(R)-7-[5-(4-Fluoro-benzyl)-[1,2,3]triazol-1-yl]-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl}-acetic acid | HCID 46892777 | — |
Reaction Steps
The title compound was prepared using enantiomerically pure propyl (7-azido-6,7,8,9-tetrahydropyrido[1,2-α]indol-10-yl)acetate from EXAMPLE 6 and 1-fluoro-4-prop-2-yn-1-ylbenzene prepared from 4-fluorobenzyl chloride and ethynyltrimethylsilane described in EXAMPLE 8 EXAMPLE 28.1 and 28.2 were prepared from the chiral azide with the retention time of 10.3 and 11.5 min respectively from EXAMPLE 6. MS (+ESI) m/z: 405.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023864B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-79d4eb822e3946d893efa2353767396e |
| Source note | uspto-grants-2015_05 |