Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Sulfate | HCID 24507 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 86760923 | HCID 86760923 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | HCID 58777908 | HCID 58777908 | — |
Reaction Steps
6.4 g of tert-butyl (3R)-3-({[(1R)-1-(4-chlorobenzyl)-2-methoxy-2-oxoethyl]amino}methyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate are dissolved in 150 ml of a mixture of tetrahydrofuran/water/MeoH (1/1/1) at 0° C., and 0.99 g of lithium hydroxide hydrate is added. Stirring is maintained at 0° C. for 3 h. 0.5 g of lithium hydroxide hydrate is then added. The medium is maintained at 0° C. for 16 h. Potassium sulphate is added up to a pH of 7. The precipitate obtained is filter-dried and rinsed with diethyl ether. After drying over P2O5, 7.2 g of N-{[(3R)-2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinolin-3-yl]methyl}-4-chloro-D-phenylalanine are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569582B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-544b6de00c77482ea394406df09feb67 |
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| Source note | uspto-grants-2009_08 |
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