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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514246Generated: November 5, 2026

Hydrochloric Acid → 9-(5-{5-Chloro-6-[(1-methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride

https://huagongshe.com/reaction/1514246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1-Dimethylethyl 9-(5-{5-chloro-6-[(1-methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylateHCID 59403470—
Solvent1,4-DioxaneHCID 31275—
Product9-(5-{5-Chloro-6-[(1-methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochlorideHCID 68469076206%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1,1-dimethylethyl 9-(5-{5-chloro-6-[(1-methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (Preparation 89) (190 mg, 0.390 mmol), 4M hydrogen chloride in dioxane (1 ml, 4.00 mmol) and 1,4-dioxane (10 ml) was stirred at 60° C. overnight. The reaction mixture was cooled and a white precipitate formed. The solid was filtered off to give the product as a white solid (170 mg). MS (ES) C19H1935ClN4O3 requires 386 Found 387 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222245B2
Source datasetuspto-grants-2012_07
ORD IDord-2adad847073943b4b2a2e895c5291b3d
Source noteuspto-grants-2012_07