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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26525Generated: October 25, 2026

3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazapine → 3-ethoxy-11H-s-triazolo[3,4-b][3]benzazepine

https://huagongshe.com/reaction/26525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazapineHCID 21323525—
Reactant3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323529—
ReactantEthanol sodium ethoxideHCID 23706232—
SolventEthanolHCID 702—
Product3-ethoxy-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323356—

Reaction Steps

By a procedure similar to that described in Example 35, 0.245 g of 3-methylsulfinyl-11H-s-triazolo [3,4-b][3]benzazepine, in lieu of 3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazepine, was reacted with 1.2 ml of 1 N-sodium ethoxide/ethanol in 2 ml of ethanol to obtain 3-ethoxy-11H-s-triazolo[3,4-b][3]benzazepine as crystals. Recrystallization from acetone yielded colorless needles, melting point 143°-144° C. The infrared absorption spectrum of this product was identical with that of the compound obtained in Example 35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150139
Source datasetuspto-grants-1979_04
ORD IDord-66aacf99ccc542b9aff3e8ef366f46b2
Source noteuspto-grants-1979_04