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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398848Generated: October 30, 2026

Ethyl 7-chloro-4-oxo-1-(thiazol-2-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylate → (+)-7-[trans-3-(N-t-butoxycarbonylmethylamino)-4-methoxy-1-pyrrolidinyl]-1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/398848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 7-chloro-4-oxo-1-(thiazol-2-yl)-1,4-dihydro-1,8-naphthyridine-3-carboxylateHCID 46928270—
Reactant(+)-trans-3-(N-t-butoxycarbonylmethylamino)-4-methoxypyrrolidineHCID 70202232—
Product(+)-7-[trans-3-(N-t-butoxycarbonylmethylamino)-4-methoxy-1-pyrrolidinyl]-1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid ethyl esterHCID 70201587—

Reaction Steps

With use of 7-chloro-1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid ethyl ester obtained in Example A-1 (4) and (-)-trans-3-(N-t-butoxycarbonylmethylamino)-4-methoxypyrrolidine obtained in Example B-3, there was obtained (+)-7-[trans-3-(N-t-butoxycarbonylmethylamino)-4-methoxy-1-pyrrolidinyl]-1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid ethyl ester (amorphous) in the same manner as in Example C-1 (1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817669
Source datasetuspto-grants-1998_10
ORD IDord-60969759dd034c3da9a1752e2b45247e
Source noteuspto-grants-1998_10