HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867987Generated: October 26, 2026
Water → 4-(2-Isopropylaminoethylamino)benzenesulfonic acid 2-acetylaminobenzothiazol-6-yl ester
https://huagongshe.com/reaction/1867987
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-acetylaminobenzothiazol-6-yl ester | HCID 57980798 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-(2-Isopropylaminoethylamino)benzenesulfonic acid 2-acetylaminobenzothiazol-6-yl ester | HCID 57980852 | 53.3% |
Reaction Steps
A solution of 4-fluorobenzenesulfonic acid 2-acetylaminobenzothiazol-6-yl ester (intermediate 64) (66 mg, 0.180 mmol), N-isopropylethylenediamine (55.2 mg, 0.540 mmol) and cesium carbonate (58.6 mg, 0.180 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 43 mg of 4-(2-isopropylaminoethylamino)benzenesulfonic acid 2-acetylaminobenzothiazol-6-yl ester (white powder) in a yield of 53%.
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-337a1e80b41c441cb15c49afe1f533f2 |
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| Source note | uspto-grants-2009_12 |
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