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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(d)thiazol-2-amineHCID 8706—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantHCID 19969579HCID 19969579—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67711381HCID 6771138196.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607934
Source datasetuspto-grants-1997_03
ORD IDord-0c6600db53ac42138207b9989ff91584
Source noteuspto-grants-1997_03