HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974865Generated: October 29, 2026
Benzo(d)thiazol-2-amine → HCID 67711381, compound
https://huagongshe.com/reaction/974865
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzo(d)thiazol-2-amine | HCID 8706 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | HCID 19969579 | HCID 19969579 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67711381 | HCID 67711381 | 96.6% |
Reaction Steps
1.09 g of dicyclohexylcarbodiimide was added to 25 ml of a solution of 2.17 g of (3RS,6SR)-3-benzyl-1-benzyloxy-3-carboxy-6-isobutylpiperazine-2,5-dione and 0.63 g of N-hydroxysuccinimide in anhydrous dioxane. The mixture was stirred at room temperature for 2 hours. Thereto was added 0.80 g of 2-aminobenzothiazole. The mixture was stirred at room temperature for 23 hours. The reaction mixture was diluted with 200 ml of ethyl acetate. The resulting solution was washed with an aqueous solution saturated with sodium hydrogen carbonate and an aqueous solution saturated with sodium chloride, then dried with anhydrous magnesium sulfate, and subjected to distillation to remove the solvent. The residue was crystallized using ethyl acetate, to obtain 2.77 g of (3RS,6SR)-3-(benzothiazol-2-yl)-carbamoyl-3-benzyl-1-benzyloxy-6-isobutylpiperazine-2,5-dione as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05607934 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-0c6600db53ac42138207b9989ff91584 |
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| Source note | uspto-grants-1997_03 |
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