Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | L-7-Hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid | HCID 2733173 | — |
| Product | HCID 66719276 | HCID 66719276 | 89% |
Reaction Steps
Thionyl chloride (1.629, 13.6 mmol) was added dropwise to a solution of (3S)-7-hydroxy-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid (0.75 g, 3.9 mmol) in methanol (30 mL) at about 0° C. under N2. The solution was warmed to about 25° C. and stirred for about 6 h, then was concentrated. The residue was washed with ether, followed by 1:1 ether pentane and dried under vacuum to yield 0.85 g of product as a white solid (89% yield). 1H NMR (d6DMSO) δ 3.09 (m, 2H); 3.78 (s, 3H); 4.23 (apparent s, 2H); 4.51 (m, 1H); 6.61 (s, 1H); 6.72 (d, J=3 Hz, 1H); 7.04 (d, J=3 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323215B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-20ddd3d9707b494e9d61dcb1da86b439 |
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| Source note | uspto-grants-2001_11 |
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