HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789515Generated: October 30, 2026
2-Chlorobenzothiazole → HCID 14049023, compound
https://huagongshe.com/reaction/1789515
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzothiazole | HCID 11987 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | Calciumoxide | HCID 6850728 | — |
| Reactant | HCID 21241578 | HCID 21241578 | — |
| Product | HCID 14049023 | HCID 14049023 | 39.7% |
Reaction Steps
A mixture of 4 parts of 1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-α-methyl-4-piperidinemethanamine, 2.7 parts of 2-chlorobenzothiazole, 1.5 parts of calcium oxide and 18 parts of N,N-dimethylacetamide was stirred for 4 hours at 140° C. The whole was filtered and to the filtrate was added 4-methyl-2-pentanone. The whole was washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichoromethane and methanol (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the ethanedioate salt in ethanol and acetonitrile. The salt was filtered off and dried, yielding 3.4 parts (39.7%) of N-[1-[1-[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]-4-piperidinyl]ethyl]-2-benzothiazolamine ethanedioate(1:2); mp. 179.6° C. (compound 60).
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-45b8253e9c01479cbece5ecd18a962aa |
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| Source note | uspto-grants-1987_08 |
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