HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867992Generated: October 26, 2026
Butyric Acid → 4-Fluorobenzenesulfonic acid 2-butyrylaminobenzothiazol-6-yl ester
https://huagongshe.com/reaction/1867992
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butyric Acid | HCID 264 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 4-Fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl ester | HCID 57980814 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Fluorobenzenesulfonic acid 2-butyrylaminobenzothiazol-6-yl ester | HCID 57980796 | 129.9% |
Reaction Steps
A solution of 4-fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl ester (intermediate 16) (359 mg, 1.107 mmol), butyric acid (146 mg, 1.66 mmol), HATU (631 mg, 1.66 mmol) and N,N-diisopropylethylamine (0.286 ml, 1.66 mmol) in 5.5 ml of dimethylformamide in a 20 ml round-bottomed flask, equipped with a magnetic bar, is stirred for 8 hours at 60° C. and then left overnight at room temperature. The reaction medium is extracted with ethyl acetate and washed with water and then with 0.1 N hydrochloric acid solution. The organic phase is dried over magnesium sulfate, filtered and then evaporated to dryness. The residue obtained (567 mg of pale yellow solid) is purified by chromatography on a 40 g Biotage silica cartridge, eluting with a 9/1 toluene/isopropanol mixture. After evaporating off the solvent, 239 mg of 4-fluorobenzenesulfonic acid 2-butyrylaminobenzothiazol-6-yl ester are obtained (white solid) in a yield of 55%.
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-9702059288db4991bb0b4cd14f60b63c |
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| Source note | uspto-grants-2009_12 |
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