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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175786Generated: November 1, 2026

Cyanomethylenetributylphosphorane → Benzyl 9a-methyl-3-((S)-3-methyl-1-oxoisochroman-6-yl)hexahydropyrazino[2,1-c][1,4]oxazine-8(1H)-carboxylate

https://huagongshe.com/reaction/2175786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanomethylenetributylphosphoraneHCID 4622928—
Reactantbenzyl 4-(2-hydroxy-2-((S)-3-methyl-1-oxoisochroman-6-yl)ethyl)-3-(hydroxymethyl)-3-methylpiperazine-1-carboxylateHCID 86727035—
SolventBenzeneHCID 241—
ProductBenzyl 9a-methyl-3-((S)-3-methyl-1-oxoisochroman-6-yl)hexahydropyrazino[2,1-c][1,4]oxazine-8(1H)-carboxylateHCID 86727034—

Reaction Conditions

Temperature135 °C

Reaction Steps

The mixture of benzyl 4-(2-hydroxy-2-((S)-3-methyl-1-oxoisochroman-6-yl)ethyl)-3-(hydroxymethyl)-3-methylpiperazine-1-carboxylate (762 mg, 1.60 mmol) and cyanomethylenetributylphosphorane (471 mg, 1.90 mmol) in dry benzene was degassed and heated to 135° C. in a microwave reactor for 3.5 h. After which point, the reaction mixture was cooled down to rt, concentrated to dryness and purified on silica gel to afford the title compound (cis or trans): MS: m/e 451.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062070B2
Source datasetuspto-grants-2015_06
ORD IDord-b049ce2e143a4fde907573ba5585dd99
Source noteuspto-grants-2015_06