Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779669Generated: October 31, 2026

(2s)-Glycidyl indol-4-yl ether → HCID 57133432, compound

https://huagongshe.com/reaction/1779669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2s)-Glycidyl indol-4-yl etherHCID 10943254—
ReactantHCID 21268353HCID 21268353—
SolventDimethyl sulfoxide methanolHCID 22036561—
ProductHCID 57133432HCID 57133432—

Reaction Steps

The title compound was prepared in a fashion similar to that described in Example 193 from 6,7-dichloro-3-(piperidin-4-yl)-1H-indole (0.80 g, 3.0 mmol) and (S)-(+)-4-(oxiranylmethoxy)-1H-indole (0.58 g, 3.1 mmol). The product was isolated as a white solid. Yield 0.64 g (47%). mp 192°-197° C. FDMS m/e=457 (M+ of free base). α[D]589 =+6.46 (c=0.99, methanol/dimethylsulfoxide).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627196
Source datasetuspto-grants-1997_05
ORD IDord-c335f7e729ee40d7a28c523de8f4a0a8
Source noteuspto-grants-1997_05