HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399965Generated: November 4, 2026
Potassium Acetate → 2-(3-Ethylureido)-7-(pyridin-2-yl)benzothiazol-5-ylboronic acid
https://huagongshe.com/reaction/1399965
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(neopentyl glycolato)diboron | HCID 2734316 | — |
| Reactant | HCID 72724619 | HCID 72724619 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(3-Ethylureido)-7-(pyridin-2-yl)benzothiazol-5-ylboronic acid | HCID 72724483 | 88.6% |
Reaction Steps
To a stirred solution of xi (25 g, 56.1 mmol) in DMSO (250 mL) at RT was added bis(neopentylglycolato)diboron (25.2 g, 112 mmol) and KOAc (16.5 g, 168 mmol). The resulting reaction mixture was de-gassed by purging N2 for 15-20 min followed by addition of Pd(dppf)Cl2 (6.8 g, 8.4 mmol). The mixture was purged with N2 for 15-20 min and then heated to 80° C. for 90 min. The reaction was poured onto saturated NH4Cl solution (1 L). The resulting precipitate was filtered and dried under vacuum. The solid cake was taken in 2M NaOH (200 mL) and stirred for 45 min at RT. The solution was filtered and the filtrate was acidified up to pH 5-6 and the resulting solid collected by filtration to give Intermediate 1 (17 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906902B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-5a93c78a0be2407e9744a7851cffbfdb |
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| Source note | uspto-grants-2014_12 |
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