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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447413Generated: October 29, 2026

Acetic Acid → Aptazapine

https://huagongshe.com/reaction/1447413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantDiboronHCID 6328200—
Reactant2-methyl-3,4-dioxo-1,2,4,14b-tetrahydro-10H-pyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepineHCID 12837715—
SolventTetrahydrofuranHCID 8028—
ProductAptazapineHCID 51355—

Reaction Steps

348 g of 2-methyl-3,4-dioxo-1,3,4,14b-tetrahydro-10H-pyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine are added portionwise over 1 hour to 4,500 ml of tetrahydrofuran and 7,410 ml of 1-molar diborane in tetrahydrofuran while cooling with ice to 18° and stirring under nitrogen. The mixture is refluxed for 24 hours, again cooled to 5° and combined with 1,200 ml of glacial acetic acid followed by 900 ml of water. The solution is refluxed for 24 hours, evaporated and the residue taken up in 10,500 ml of methanol. The solution is again refluxed for 2 hours, evaporated, the residue dissolved in 3,000 ml of water and the pH of the solution adjusted to 14 with 1,200 ml of 10% aqueous sodium hydroxide. The mixture is extracted with diethyl ether, the extract dried, filtered and evaporated to yield the 2-methyl-1,3,4,14b-tetrahydro-10H-pyrazino[1,2-a]pyrrolo[2,1-c][ 1,4]benzodiazepine melting at 98°-100°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04316900
Source datasetuspto-grants-1982_02
ORD IDord-cf49f7fa583e4e248f0d13b218c20339
Source noteuspto-grants-1982_02