HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9145Generated: October 23, 2026
Boric Acid → 1-(6-(3-Aminophenyl)-2-benzothiazolyl)-3-ethylurea
https://huagongshe.com/en/reaction/9145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Aminophenylboric acid | HCID 21895836 | — |
| Reactant | 1-(6-Bromo-2-benzothiazolyl)-3-ethylurea | HCID 21985564 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | N,N-Dimethylformamide--water (1/1) | HCID 21962138 | — |
| Product | 1-(6-(3-Aminophenyl)-2-benzothiazolyl)-3-ethylurea | HCID 21985575 | 23.4% |
Reaction Steps
A suspension of 1-(6-bromo-2-benzothiazolyl)-3-ethylurea (0.300 g, 1.00 mmol), 3-aminophenyl boric acid (0.237 g, 1.50 mmol, 1.5 eq), and sodium bicarbonate (0.210 g, 2.50 mmol, 2.5 eq) in 8 mL of mixed solvent DMF/water (5/1) was purged with nitrogen gas. To the mixture, the catalyst Pd(PPh3)4 (0.058 g, 0.05 mmol, 0.05 eq) was added. It was purged with nitrogen gas again, and was heated at about 100° C. in a sealed tube for about 48 hours. More Pd(PPh3)4 (0.025 g, 0.02 mmol, 0.02 eq) and more boric acid (0.080 g, 0.50 mmol, 0.50 eq) were added after the first 24 hours. The mixture was taken up in MeOH, concentrated, dissolved in methylene chloride, washed with sodium bicarbonate solution, dried (MgSO4), evaporated, and purified by flash chromatography on SiO2 with MeOH and methylene chloride (1/50) to give the desired compound 0.073 g (23%). LC/MS 313.2 (M+1); LC retention time 2.11 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07091227B2 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-1d4c968dd1784c18a9903db176fc40d0 |
|---|
| Source note | uspto-grants-2006_08 |
|---|