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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019961Generated: November 1, 2026

3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylic acid → (3S,4R)-1-[2-(7-methoxy-quinoxalin-2-ylsulfanyl)-ethyl]-4-[(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carbonyl)-amino]-piperidine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1019961

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylic acidHCID 760993—
Reactant(3S,4R)-4-amino-1-[2-(7-methoxy-quinoxalin-2-ylsulfanyl)-ethyl]-piperidine-3-carboxylic acid ethyl esterHCID 66747315—
Product(3S,4R)-1-[2-(7-methoxy-quinoxalin-2-ylsulfanyl)-ethyl]-4-[(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carbonyl)-amino]-piperidine-3-carboxylic acid ethyl esterHCID 66747298—

Reaction Steps

The title compound is prepared as an orange semisolid (280 mg, 87% yield) following Scheme 3 and in analogy to Example 35 using (3S,4R)-4-amino-1-[2-(7-methoxy-quinoxalin-2-ylsulfanyl)-ethyl]-piperidine-3-carboxylic acid ethyl ester (216 mg, 0.50 mmol, 1.0 eq) and 3-oxo-3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid (113 mg, 0.50 mmol, 1.0 eq) as starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716280B2
Source datasetuspto-grants-2014_05
ORD IDord-78defb198dcb424c95202f099c425ed5
Source noteuspto-grants-2014_05