HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857657Generated: October 30, 2026
Acetic Anhydride → HCID 10433404, compound
https://huagongshe.com/reaction/857657
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 21865137 | HCID 21865137 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10433404 | HCID 10433404 | — |
Reaction Steps
To a 50 mL, round-bottomed flask containing 4-[6-(4-bromo-phenyl)-pyrimidin-4-yloxy]-benzothiazol-2-ylamine, (Example 129(c)), (0.050 g, 0.13 mmol) was added anhydrous toluene (3 mL) and acetic anhydride (0.010 mL, 0.39 mmol, Aldrich). The mixture was heated at 90° C. and the progress of the reaction was monitored by TLC (developed in 50% EtOAc/hexanes). After reaching completion, the reaction mixture was allowed to cool to room temperature, the white precipitate was collected by filtration, washed with MeOH (5 mL), and dried under vacuum to obtain the title compound as a white solid. Mp: 271–272° C. MS (ESI, pos. ion.) m/z: 441 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07144888B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-8f179bfecd684d1183de805a52cf7ca2 |
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| Source note | uspto-grants-2006_12 |
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