HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2s)-Glycidyl indol-4-yl ether → HCID 70217223, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2s)-Glycidyl indol-4-yl ether | HCID 10943254 | — |
| Reactant | HCID 21268229 | HCID 21268229 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70217223 | HCID 70217223 | — |
Reaction Steps
The title compound was prepared in a fashion similar to that described in Example 1 using (S)-(+)-4-(oxiranylmethoxy)-1H-indole (0.166 g, 0.088 mmol) and 6-chloro-2-(1,2,3,6-tetrahydropyridin-4-yl)benzo[b]thiophene (0.200 g, 0.080 mmol) using ethanol as reaction solvent. Yield 0.122 g (35%) of a tan powder. FDMS m/e=438 (M+ of free base).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05614523 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-3b5355ccc49d44199626b800c8da73df |
| Source note | uspto-grants-1997_03 |