HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Acetyl-L-leucine → N-acetyl-L-leucinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Acetyl-L-leucine | HCID 70912 | — |
| Reactant | (-)-7-Hydroxy-6-methoxy-1-(3,4-dimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline | HCID 11186519 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-acetyl-L-leucinate | HCID 6928495 | — |
| Product | (-)-7-Hydroxy-6-methoxy-1-(3,4-dimethoxybenzyl)-1,2,3,4-tetrahydroisoquinoline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04461895 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-63474b94aa8e4f1e947d66ac3f62d6c7 |
| Source note | uspto-grants-1984_07 |