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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462973Generated: October 27, 2026

N-Acetyl-L-leucine → N-acetyl-L-leucinate

https://huagongshe.com/reaction/1462973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetyl-L-leucineHCID 70912—
Reactant(-)-7-Hydroxy-6-methoxy-1-(3,4-dimethoxybenzyl)-1,2,3,4-tetrahydroisoquinolineHCID 11186519—
SolventMethanolHCID 887—
ProductN-acetyl-L-leucinateHCID 6928495—
Product(-)-7-Hydroxy-6-methoxy-1-(3,4-dimethoxybenzyl)-1,2,3,4-tetrahydroisoquinolineHCID 11186519—

Reaction Steps

18.9 g. (57.4 mmol) (±)-7-Hydroxy-6-methoxy-1-(3,4-dimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline are dissolved at 60° C. in 70 ml. methanol and mixed with a solution of 9.94 g. (57.4 mmol) N-acetyl-L-leucine in 50 ml. methanol, also heated to 60° C. The solution obtained is concentrated by evaporating in a vacuum. After the addition of isopropanol/diethyl ether and recrystallisation from the same solvent mixture, there is obtained the N-acetyl-L-leucinate of (-)-7-hydroxy-6-methoxy-1-(3,4-dimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline; m.p. 179°-186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04461895
Source datasetuspto-grants-1984_07
ORD IDord-63474b94aa8e4f1e947d66ac3f62d6c7
Source noteuspto-grants-1984_07