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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857657Generated: October 30, 2026

Acetic Anhydride → HCID 10433404, compound

https://huagongshe.com/reaction/857657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 21865137HCID 21865137—
SolventTolueneHCID 1140—
ProductHCID 10433404HCID 10433404—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144888B2
Source datasetuspto-grants-2006_12
ORD IDord-8f179bfecd684d1183de805a52cf7ca2
Source noteuspto-grants-2006_12