HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789513Generated: October 24, 2026
Sodium Carbonate → N-[[1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-4-piperidinyl]methyl]-5,6,7-trimethoxy-2-benzothiazolamine (E)-2-butenedioate
https://huagongshe.com/en/reaction/1789513
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 2,3-Dihydro-1,4-benzodioxin-2-ylmethyl methanesulfonate | HCID 263445 | — |
| Reactant | 5,6,7-trimethoxy-N-(4-piperidinylmethyl)-2-benzothiazolamine | HCID 21241614 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[[1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-4-piperidinyl]methyl]-5,6,7-trimethoxy-2-benzothiazolamine (E)-2-butenedioate | HCID 86742980 | 48.5% |
Reaction Steps
A mixture of 2.8 parts of 2,3-dihydro-1,4-benzodioxin-2-methanol methanesulfonate (ester), 3.4 parts of 5,6,7-trimethoxy-N-(4-piperidinylmethyl)-2-benzothiazolamine, 3 parts of sodium carbonate and 67.5 parts of N,N-dimethylacetamide was stirred overnight at about 75° C. Water was added. The product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the (E)-2-butenedioate salt in ethanol and 2-propanone. The salt was filtered off and dried, yielding 3.2 parts (48.5%) of N-[[1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-4-piperidinyl]methyl]-5,6,7-trimethoxy-2-benzothiazolamine (E)-2-butenedioate(2:3); mp. 171.6° C. (compound 26).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04689330 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-e5b173451e7142968c31ab748f8e6b09 |
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| Source note | uspto-grants-1987_08 |
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