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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710371Generated: November 2, 2026

Ammonia → HCID 178426724, compound

https://huagongshe.com/reaction/1710371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantN-(2-fluoro-4-methyl-phenyl)-4-{2-[2-(7-thioxo-azepan-2-yl)-ethyl]-3H-imidazo[4,5-b]pyridin-6-yl}-benzenesulfonamideHCID 178426726—
ReactantHCID 178508386HCID 178508386—
SolventMethanolHCID 887—
ProductHCID 178426724HCID 178426724—

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 100 mg of N-(2-fluoro-4-methyl-phenyl)-4-{2-[2-(7-thioxo-azepan-2-yl)-ethyl]-3H-imidazo[4,5-b]pyridin-6-yl}-benzenesulfonamide (compound A8) and 4.30 ml of methanol containing ammonia (strength: 7.0 M) at 50° C. for 90 hours. Subsequently, the mixture is filtered with suction. The residue is washed with 20 ml of methanol and dried under high vacuum to afford 61 mg of the pure title compound as an amorphous, colorless solid of m.p. 265° C. ESI-MS: 521.2 (MH+), TLC: Rf=0.28 (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-280f094ba0444251b9ed0f86bfd5a7d4
Source noteuspto-grants-2010_09