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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15321Generated: October 26, 2026

3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carbaldehyde → 3-Chloro-4-[(4-{[(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)methyl]amino}-1-piperidinyl)methyl]-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one Hydrochloride

https://huagongshe.com/reaction/15321

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carbaldehydeHCID 10773638—
Reactant4-[(4-Amino-1-piperidinyl)methyl]-3-chloro-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-oneHCID 57707475—
Product3-Chloro-4-[(4-{[(3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl)methyl]amino}-1-piperidinyl)methyl]-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one HydrochlorideHCID 6868562569%

Reaction Steps

The free base of the title compound was synthesised from 4-[(4-amino-1-piperidinyl)methyl]-3-chloro-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one and 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6-carboxaldehyde (for a synthesis see WO2002056882, Example 5(b)), according to the general method of Example 2(h), in 69% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732461B2
Source datasetuspto-grants-2010_06
ORD IDord-d7c270c11b2d48df9ab6c3a0d6b5eae8
Source noteuspto-grants-2010_06