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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898867Generated: October 26, 2026

Dimethylformamide → Cis(+)-3-acetyloxy-2,3-dihydro-5-(2-methyl-3-dimethylaminopropyl)-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one oxalate

https://huagongshe.com/reaction/1898867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Bromo-3-chloro-2-methylpropaneHCID 95566—
Reactant(2S)-cis-3-(Acetyloxy)-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-oneHCID 11110671—
SolventAmmonium ChlorideHCID 25517—
ProductCis(+)-3-acetyloxy-2,3-dihydro-5-(2-methyl-3-dimethylaminopropyl)-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one oxalateHCID 67766488—

Reaction Conditions

Temperature-7 °C

Reaction Steps

5 g cis(+)-3-acetyloxy-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one were dissolved in 30 ml dimethylformamide, cooled at -7° C. 1.4 g 88% KOH and, after 10 minutes, 3.8 g 1-bromo-3-chloro-2-methylpropane were slowly added. The temperature was then raised to 0° C. and the mixture was stirred for 4 hours. The reaction mixture was then poured in 250 ml 0.6N NH4Cl solution and extracted with CH2Cl2. The collected organic phases were washed with H2O, dried on Na2SO4 and evaporated under reduced pressure. 6.4 g a thick orange oil were obtained and were dissolved in hot isopropyl alcohol. A crystalline solid precipitated by cooling, m.p. 100°-103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571807
Source datasetuspto-grants-1996_11
ORD IDord-31a6cb7d33ac478aa99f33ea1dc5e737
Source noteuspto-grants-1996_11