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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710372Generated: October 31, 2026

Ammonia → HCID 178424386, compound

https://huagongshe.com/reaction/1710372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 178424388HCID 178424388—
ReactantHCID 178508386HCID 178508386—
SolventMethanolHCID 887—
ProductHCID 178424386HCID 178424386—

Reaction Steps

The title compound is synthesized as described for 7-[2-(6-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-4,5,6,7-tetrahydro-3H-azepin-2-ylamine (compound 1) from 71 mg of 4-{2-[2-(7-thioxo-azepan-2-yl)-ethyl]-3H-imidazo[4,5-b]pyridin-6-yl}-N-o-tolyl-benzenesulfonamide (compound A9) and 3.2 ml of methanol containing ammonia (strength: 7.0 M) at 50° C. for 66 hours. Subsequently, the solution is concentrated in vacuo to yield 60 mg of the pure title compound as an amorphous, colorless solid of m.p. 215° C. ESI-MS: 503.4 (MH+), TLC: Rf=0.25 (HPTLC RP-C18; acetonitrile/water 2:1 parts by volume).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790710B2
Source datasetuspto-grants-2010_09
ORD IDord-543b972b5c084da9a1da10ae7d7ec664
Source noteuspto-grants-2010_09