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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164341Generated: October 30, 2026

3-Ethoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxamide → 3-Ethoxy-4-phenyl-4H-furo[3,2-b]indole-2-carbonitrile

https://huagongshe.com/reaction/2164341

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxamideHCID 13220398—
SolventWaterHCID 962—
Product3-Ethoxy-4-phenyl-4H-furo[3,2-b]indole-2-carbonitrileHCID 1339416491%

Reaction Steps

Prepared by the procedure described in Example 21 from 6.5 g (0.020 mole) of 3-ethoxy-4-phenyl-4H-furo[3,2-b]indole-2-carboxamide. The crude product (5.5 g, 90% yield), after being washed with water and dried, was converted to the corresponding tetrazole without additional purification. A portion of the crude nitrile recrystallized from methanol yielded an analytically pure sample, mp 121°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04503236
Source datasetuspto-grants-1985_03
ORD IDord-ffc6f526c5034650bf80ee33eb650126
Source noteuspto-grants-1985_03