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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447403Generated: October 31, 2026

Allyl bromide → HCID 12837724, compound

https://huagongshe.com/reaction/1447403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 12837720HCID 12837720—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 12837724HCID 12837724—

Reaction Steps

To the solution of 4.8 g of 1,3,4,14b-tetrahydro-2H,10H-pyrazino[1,2-a]pyrrolo[2,1-c][1,4]-benzodiazepine in 20 ml of dimethyl formamide and 2.44 g of triethylamine, 2.91 g of allyl bromide are added dropwise while stirring. After one hour, the mixture is diluted with diethyl ether, washed with water and saturated aqueous sodium chloride and the aqueous phase is once more extracted with diethyl ether. The combined organic solutions are washed with saturated aqueous sodium bicarbonate, dried, evaporated and the residue triturated with diethyl ether, to yield the 2-allyl-1,3,4,14b-tetrahydro-10H--pyrazino[1,2-a]pyrrolo[2,1-c][1,4]-benzodiazepine melting at 130°-132°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04316900
Source datasetuspto-grants-1982_02
ORD IDord-e55f1d5ad3e44a088158210febfe449b
Source noteuspto-grants-1982_02