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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743643Generated: November 2, 2026

N,N-diethylazetidin-3-amine dihydrochloride → 8-(3-Diethylamino-1-azetidinyl)-3-ethoxy-carbonyl-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine

https://huagongshe.com/reaction/743643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-diethylazetidin-3-amine dihydrochlorideHCID 19423807—
Reactant3-Ethoxy-carbonyl-7,8-difluoro-1-methyl-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridineHCID 86749213—
Product8-(3-Diethylamino-1-azetidinyl)-3-ethoxy-carbonyl-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridineHCID 86749833—

Reaction Steps

8-(3-Diethylamino-1-azetidinyl)-3-ethoxy-carbonyl-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine was prepared under the conditions of Example 2, but starting with 2 g of 3-ethoxy-carbonyl-7,8-difluoro-1-methyl-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine and 1.4 g of 3-(diethylamino)-azetidine dihydrochloride. After recrystallization of the crude product in 500 cm3 of methanol, 2.07 g of 8-(3-diethylamino-1-azetidinyl)-3-ethoxy-carbonyl-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine are obtained in the form of a yellow solid, melting point 260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556861
Source datasetuspto-grants-1996_09
ORD IDord-98b6e52e90ed481485a972f3eddf7798
Source noteuspto-grants-1996_09