Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | L-Alanine | HCID 5950 | — |
| Reactant | HCID 66713022 | HCID 66713022 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Product | HCID 57473370 | HCID 57473370 | 59% |
Reaction Steps
A mixture of 4-Hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carboxylic acid butyl ester (176 mg, 0.5 mmol), (S)-alanine (225 mg, 2.5 mmol) and a 0.5 N solution of MeONa in MeOH (5 ml, 2.5 mmol) was heated in a microwave oven with stirring for 20 min at 120° C. before the mixture was concentrated in vacuo. To the residue was added water (15 ml) and the mixture was washed with Et2O (3×30 ml). The so purified aq. solution was acidified by the addition of 6 N HCl and extracted with EtOAc (1×30 ml). The organic phase was dried over MgSO4 and concentrated in vacuo to give the title compound as a tan solid (108 mg); MS-(−)-ion M−1=365.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629357B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-5b97754ba9fe49549a4279f2c3b9a087 |
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| Source note | uspto-grants-2009_12 |
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