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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059271Generated: October 30, 2026

methyl 10H-pyrazino[2,3-b][1,4]benzothiazine-8-carboxylate → 10H-Pyrazino[2,3-b][1,4]benzothiazine-8-methanol

https://huagongshe.com/reaction/1059271

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 10H-pyrazino[2,3-b][1,4]benzothiazine-8-carboxylateHCID 11747308—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product10H-Pyrazino[2,3-b][1,4]benzothiazine-8-methanolHCID 1094429254.1%

Reaction Steps

259 g of methyl 10H-pyrazino[2,3-b][1,4]benzothiazine-8-carboxylate was dissolved in a solvent mixture of 3 l of methylene chloride with 0.5 l of tetrahydrofuran under a nitrogen atmosphere. Next, 2.5 l of a 1.01 M solution of diisobutylaluminum hydride in toluene was added dropwise thereinto while cooling the mixture so as to maintain the temperature in the system at 15° C. or below. After the completion of the reaction, the reaction mixture was poured into a mixture of 5 kg of ice with 3 l of methylene chloride. After adding 5 l of tetrahydrofuran, the resulting mixture was stirred for 1 hour. Then it was filtered and the filtrate was washed with water. After distilling off the solvent under reduced pressure, the obtained crystals were washed with diisopropyl ether to thereby give 125 g of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-3f864d6da12b4e30b0ec37d215ec8f6f
Source noteuspto-grants-2003_02