HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867986Generated: October 26, 2026
Acetic Acid → 4-Fluorobenzenesulfonic acid 2-acetylaminobenzothiazol-6-yl ester
https://huagongshe.com/reaction/1867986
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 4-Fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl ester | HCID 57980814 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Fluorobenzenesulfonic acid 2-acetylaminobenzothiazol-6-yl ester | HCID 57980798 | 58% |
Reaction Steps
A solution of 4-fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl ester (intermediate 16) (101.2 mg, 0.312 mmol), acetic acid (56.2 mg, 0.936 mmol), HBTU (355 mg, 0.936 mmol) and N,N-diisopropylamine (326 μl, 1.872 mmol) in 5 ml of dimethylformamide in a test tube, equipped with a magnetic bar, is stirred for 20 hours at room temperature. 100 ml of water are added and the reaction medium is extracted with ethyl acetate. The organic phase is dried over magnesium sulfate and evaporated. The residue obtained is taken up in ethyl acetate and purified on a Varian flash cartridge containing 5 g of silica of porosity 15-35μ, with a mixture of 1% methanol in dichloromethane. After evaporating off the solvent, 66 mg of 4-fluorobenzenesulfonic acid 2-acetylaminobenzothiazol-6-yl ester are obtained (yellow oil) in a yield of 58%. LC/MS (method A1): [M+H]+: 367.14, retention time: 3.50 min.
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-532438e75dd54a26acddd3c467af2c0a |
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| Source note | uspto-grants-2009_12 |
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