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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220227Generated: November 1, 2026

Pyridine → HCID 69196730, compound

https://huagongshe.com/reaction/2220227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 68965888HCID 68965888—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
ProductHCID 69196730HCID 6919673096%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of 9-Bromo-2-chloro-11,12-dihydro-6H-5-oxa-12-aza-dibenzo[a,e]cyclooctene Example 347E (3.8 mg, 11.7 umol) and DMAP (cat. amount) in toluene (0.3 mL) was added acetic anhydride (0.10 mL, 1.05 mmol) and pyridine (0.05 mL, 46.9 umol). This reaction mixture was heated at 70° C. for 30 minutes, cooled to room temperature and concentrated in vacuo. This was purified by a ISCO auto CombiFlash with a RediSep 4 g column, eluted with Hexane-CH2Cl2, detected at 220 nM to give 4.1 mg of 1-(9-Bromo-2-chloro-6,11-dihydro-5-oxa-12-aza-dibenzo[a,e]cycloocten-12-yl)-ethanone Example 347E in 96% yield. HPLC Rt=3.56 min (YMC S5 ODS column 4.6×50 mm, 10-90% aqueous methanol over 4 minutes containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm) LC/MS: M+H=366.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417040B2
Source datasetuspto-grants-2008_08
ORD IDord-67ef38d3a57b4dddaf15e8a29a8693da
Source noteuspto-grants-2008_08