HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867990Generated: November 1, 2026
Water → 4-(2-Isopropylaminoethylamino)benzenesulfonic acid 2-(cyclopentanecarbonyl-amino)benzothiazol-6-yl ester
https://huagongshe.com/reaction/1867990
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | N-Isopropylethylenediamine | HCID 88098 | — |
| Reactant | 4-Fluorobenzenesulfonic acid 2-(2-methoxy-acetylamino)benzothiazol-6-yl ester | HCID 57980854 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-(2-Isopropylaminoethylamino)benzenesulfonic acid 2-(cyclopentanecarbonyl-amino)benzothiazol-6-yl ester | HCID 57980839 | 48.7% |
Reaction Steps
A solution of 4-fluorobenzenesulfonic acid 2-(2-methoxyacetylamino)-benzothiazol-6-yl ester (intermediate 68) (90 mg, 0.214 mmol), N-isopropylethylenediamine (65.6 mg, 0.642 mmol) and cesium carbonate (69.7 mg, 0.214 mmol) in 2 ml of dimethyl sulfoxide in a test tube, equipped with a magnetic bar, is stirred overnight at 80° C. 100 ml of water are added and the reaction medium is extracted with ethyl acetate. The organic phase is then washed with water, dried over magnesium sulfate and evaporated. The residue, purified by LC/MS, gives 26.2 mg of 4-(2-isopropylaminoethylamino)benzenesulfonic acid 2-(cyclopentanecarbonyl-amino)benzothiazol-6-yl ester (white powder) in a yield of 24%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07632952B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-5b5b3b01394f45129a079e55ce8a809f |
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| Source note | uspto-grants-2009_12 |
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