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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425230Generated: October 27, 2026

Methanol → Olanzapine

https://huagongshe.com/reaction/425230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant1-MethylpiperazineHCID 53167—
Reactant10H-Thieno[2,3-b][1,5]benzodiazepin-4-amine, 2-methyl-, hydrochloride (1:1)HCID 135525650—
SolventDimethyl SulfoxideHCID 679—
ProductOlanzapineHCID 135398745—

Reaction Conditions

Temperature20 °C

Reaction Steps

4-amino-2-methyl-10H-thieno[2,3-b][1,5]benzodiazepine, hydrochloride (50 g) was stirred in a mixture of N-Methylpiperazine (113 g) and Dimethylsulfoxide (300 mL) at 120° C. for 20 h under nitrogen atmosphere. The reaction mass was cooled to 20° C., followed by addition of methanol (500 mL) and the reaction mass was stirred for 30 min. Water (150 mL) was added at 20° C. in 25 min, and the reaction mass was cooled to 5° C. The reaction mass was stirred for 30 min at 0-5° C. The product was filtered and was washed with chilled methanol (50 mL, 5° C.). Dried the product at 50° C. under reduced pressure to give technical 2-Methyl-4-(4-methyl-1-piperazinyl)-10H-thieno[2,3-b][1,5]benzodiazepine or Olanzapine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106188B2
Source datasetuspto-grants-2012_01
ORD IDord-52f8738321334c25b136f78313dd4dc0
Source noteuspto-grants-2012_01