HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9110Generated: October 25, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → 1-(7-Hydroxy-2-benzothiazolyl)-3-ethyl-urea
https://huagongshe.com/reaction/9110
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 1-(6,6-Dibromo-7-oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-urea | HCID 21985529 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(7-Hydroxy-2-benzothiazolyl)-3-ethyl-urea | HCID 21985523 | 32.2% |
Reaction Steps
To a suspension of 1-(6-bromo-7-oxo-4,5,6,7-tetrahydro-2-benzothiazolyl)-3-ethyl-urea 5 (0.100 g, 0.314 mmol) in THF (1.0 mL) was added DBU (0.141 mL, 0.94 mmol, 3 eq) dropwise at about 20° C. A dark green suspension was obtained while heat was generated upon addition of DBU. It was stirred at about 20° C. for about 18 hours. The reaction mixture was concentrated and dissolved in DMF (2 mL). LC/MS purification gave 0.024 g (32%) of the desired compound 8. 1H NMR (DMSO) δ 10.54 (br s, 1H, NH), 7.17–7.07 (m, 2H, ArH), 6.63 (d, 1H, J=6.9 Hz, ArH), 6.70 (br s, 1H, NH), 3.18 (m, 2H, CH2), 1.09 (t, 3H, J=7.2 Hz, CH3). LC/MS 238 (MH+); RP-HPLC RT 2.26 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091227B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-f28c76dea7f44a58b87eb28465351440 |
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| Source note | uspto-grants-2006_08 |
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