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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803364Generated: October 25, 2026

Benzyloxy-3-nitro[1,5]naphthyridin-4-amine → Benzyloxyquinoline-3,4-diamine

https://huagongshe.com/reaction/1803364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxy-3-nitro[1,5]naphthyridin-4-amineHCID 66649873—
ReactantBenzyloxy-3-nitroquinolin-4-amineHCID 66649911—
ProductBenzyloxyquinoline-3,4-diamineHCID 66958435—
ProductBenzyloxy[1,5]naphthyridine-3,4-diamineHCID 67157263—

Reaction Steps

In steps (6) and (7) of Reaction Scheme V, a benzyloxy-3-nitroquinolin-4-amine or benzyloxy-3-nitro[1,5]naphthyridin-4-amine of Formula LVI is reduced to provide a benzyloxyquinoline-3,4-diamine or benzyloxy[1,5]naphthyridine-3,4-diamine of Formula LVII, which is then is treated with a halogen-substituted carboxylic acid equivalent to provide a benzyloxy-1H-imidazo[4,5-c]quinoline or benzyloxy-1H-imidazo[4,5-c][1,5]naphthyridine of Formula LVIII. Steps (6) and (7) of Reaction Scheme V can be carried out according to the methods described in steps (2) and (3) of Reaction Scheme I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350034B2
Source datasetuspto-grants-2013_01
ORD IDord-14dddab6a92e49f693c5ddcbccd3852a
Source noteuspto-grants-2013_01