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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575454Generated: October 30, 2026

Ammonia → 9-Bromo-4,5-dihydrobenzo[b]pyrazolo[1,5-d][1,4]oxazepine-2-carboxamide

https://huagongshe.com/reaction/575454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthyl 9-bromo-4,5-dihydrobenzo[b]pyrazolo[1,5-d][1,4]oxazepine-2-carboxylateHCID 58204733—
Product9-Bromo-4,5-dihydrobenzo[b]pyrazolo[1,5-d][1,4]oxazepine-2-carboxamideHCID 5820433089%

Reaction Conditions

Temperature122.5 °C

Reaction Steps

A suspension of ethyl 9-bromo-4,5-dihydrobenzo[b]pyrazolo[1,5-d][1,4]oxazepine-2-carboxylate (compound 61-4, page 196, WO 2011/036280) (0.3 g, 0.89 mmol) in 7 M ammonia solution (in methanol, 4 ml) was heated in a microwave apparatus to 120-125° C. for 2.5 hours. After cooling the mixture was left at room temperature for 18 hours before the solvent was removed in vacuo and the residue was then taken up in tetrahydrofuran and pre-absorbed onto a small amount of silica. Purification by FCC (silica, 20-100% ethyl acetate in heptane) gave 245 mg (89%) of the title compound. 1H NMR (250 MHz, DMSO-d6) 8 ppm 3.18 (2H, t, J=5.79 Hz), 4.46 (2H, t, J=5.79 Hz), 6.71 (1H, s), 7.18 (1H, dd, J=8.60, 0.69 Hz), 7.39 (1H, br, s.), 7.51 (1H, ddd, J=8.68, 2.44, 0.76 Hz), 7.84 (1H, br. s.), 8.19 (1H, dd, J=2.44, 0.76 Hz)); M+1=308/310.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-436693777cfc49329d442a917dd98ae3
Source noteuspto-grants-2015_05