Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | HCID 15386083 | HCID 15386083 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178455162 | HCID 178455162 | 73.1% |
Reaction Steps
A mixture of 9.8 g of guanidine free base and 13.8 g of 2-methoxy-3-carboethoxy-5-[t-butyl(dimethyl)silyloxymethyl]-3,4,5,6-tetrahydropyridine was heated at 90° C. under nitrogen for 18 hours. The mixture was cooled to room temperature, and water was added to give a white precipitate. This was filtered to give 9.5 g of the title compound: MS m/z 311 (M+ +1), 310 (M+); 300-MHz 1H NMR (DMSO-d6) δ0.03 (s, 6 H), 0.85 (S, 9 H), 1.70-1.88 (m, 2 H), 2.27-2.38 (m, 1 H), 2.78-2.88 (m, 1 H), 3.16-3.27 (m, 1 H), 3.37-3.45 (m, 1 H), 3.49-3.58 (m, 1 H), 5.92 (b s, 2 H), 6.21 (b s, 1 H), 9.67 (b s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05159079 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-b61d22809da5484eb56cc7f117e8c29e |
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| Source note | uspto-grants-1992_10 |
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