Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylhomoveratrylamine | HCID 77039 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 12462834 | HCID 12462834 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 57010-32-9 | HCID 6917759 | — |
Reaction Steps
10.4 g of 2-(3-chloropropyl)-2-(3,4-dimethoxyphenyl)-m-dithiane-1,1,3,3-tetraoxide are treated with 5.11 g of N-methyl-homoveratrylamine, 30 ml of N-ethyl-N,N-diisopropylamine and 70 ml of dimethylformamide. The solution is heated at 120° C for 6 hours. After evaporation, the residue is worked-up in a manner analogous to that described in Example 5. There is obtained N-(3,4-dimethoxyphenethyl)-2-(3,4-dimethoxyphenyl)-N-methyl-m-dithiane-2-propylamine-1,1,3,3-tetraoxide hydrochloride of melting point 167°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04073797 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-6c72fd74688d4533917c0c4effe7c69e |
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| Source note | uspto-grants-1978_02 |
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