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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649331Generated: October 28, 2026

HCID 14809494, compound → HCID 20143011, compound

https://huagongshe.com/reaction/649331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14809494HCID 14809494—
ReactantHCID 20143023HCID 20143023—
ReactantHCID 86742111HCID 86742111—
ProductHCID 20143011HCID 2014301172%
ProductHCID 20143097HCID 2014309712.8%
ProductHCID 20143168HCID 2014316864.9%

Reaction Steps

3,4-Dihydro-2-(2-hydroxy-5-methoxyphenyl)-4-methyl-2-methylthio-3-oxo-2H-1,4-benzothiazine (5.2 g, compound No. 8), β-chloropropionaldehyde diethyl acetate (3.0 g) and N-methyl-2-(3,4-dimethoxyphenyl)propylamine hydrochloride (5.2 g) are treated by the similar method as in Example 26 to give 4.7 g (64.9%) of 2-[2-(3,3-diethoxypropoxy)-5-methoxyphenyl]-3,4-dihydro-4-methyl-2-methylthio-3-oxo-2H-1,4-benzothiazine (compound No. 21, (IR: neat, cm-1) 1660, 1555, 1048, 750), 2.8 g (72.0%) of 3,4-dihydro-2-[5-methoxy-2-(3-oxopropoxy)phenyl]-4-methyl-2-methylthio-3-oxo-2H-1,4-benzothiazine (compound No. 22, (IR: neat, cm-1) 1722, 1658, 1588, 1036, 748) and 0.6 g (12.8%) of the titled compound (mp. 153°-156.5° C. (dec.)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04739050
Source datasetuspto-grants-1988_04
ORD IDord-29f48d8f315246dc918b6e4e7ecb102d
Source noteuspto-grants-1988_04