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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455012Generated: October 27, 2026

1-Hydroxybenzotriazole → 2-[3-(4-Chloro-phenyl)-ureido]-benzothiazole-6-carboxylic acid (2-oxo-2,3-dihydro-benzooxazol-6-yl)-amide

https://huagongshe.com/reaction/455012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant6-amino-1,3-benzoxazol-2(3H)-oneHCID 826989—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-[3-(4-Chloro-phenyl)-ureido]-benzothiazole-6-carboxylic acidHCID 86661381—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[3-(4-Chloro-phenyl)-ureido]-benzothiazole-6-carboxylic acid (2-oxo-2,3-dihydro-benzooxazol-6-yl)-amideHCID 4694055070%

Reaction Steps

Starting material 35 (300 mg, 45% content, 0.4 mmol) and 6-Amino-3H-benzooxazol-2-one (30, 58 mg, 0.4 mmol) were dissolved in 2 ml of dry DMF. Then EDCl (96 mg, 0.5 mmol) and HOBt (76 mg, 0.5 mmol) were added. The reaction was stirred at ambient temperature over night. It was then purred into water and the resulting precipitate was filtered. The isolated precipitate was then stirred in 100 ml warm methanol and the non-soluble crystals filtered and washed with methanol. Thereby the desired product 36 (130 mg, 0.271 mmol, 70%) could be isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497283B2
Source datasetuspto-grants-2013_07
ORD IDord-d1ab1390220a4213af605416c18756cd
Source noteuspto-grants-2013_07