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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345570Generated: October 30, 2026

Tetrahydrofuran → HCID 15096965, compound

https://huagongshe.com/reaction/345570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 19883518HCID 19883518—
CatalystMercuric oxideHCID 30856—
SolventAcetonitrileHCID 6342—
ProductHCID 15096965HCID 15096965—

Reaction Steps

A mixture of 7.3 parts of N-(3-amino-4-pyridinyl)-N'- methylthiourea, 15 parts of mercury (II)oxide, 90 parts of tetrahydrofuran and 80 parts of acetonitrile was stirred and refluxed for 20 hours. The reaction mixture was filtered hot over Hyflo and the filter-cake was washed with 240 parts of boiling ethanol. The filtrate was evaporated in vacuo and the residue was boiled in acetonitrile. The product was filtered off and dried, yielding 5 parts of N-methyl-3H-imidazo[4,5-c]pyridin-2-amine; mp. 255.7° C. (intermediate 96).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057525
Source datasetuspto-grants-1991_10
ORD IDord-27f5937c3a0a45b3b6e3d7d8e57c69cb
Source noteuspto-grants-1991_10