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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473899Generated: October 30, 2026

Trifluoroacetic acid → HCID 69675378, compound

https://huagongshe.com/reaction/473899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70815046HCID 70815046—
SolventChloroformHCID 6212—
ProductHCID 69675378HCID 69675378117.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1,1-dimethylethyl 7-(1-{[(2-methylpropyl)oxy]carbonyl}-1H-imidazo[4,5-b]pyridine-6-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (0.40 g, 0.86 mmol) in chloroform (4 mL) was added dropwise trifluoroacetic acid (5 mL) and the solution then warmed to 80° C. for 45 minutes. After cooling, the solution was concentrated and dried to give 2-methylpropyl 6-(2,3,4,5-tetrahydro-1,4-benzoxazepin-7-yl)-1H-imidazo[4,5-b]pyridine-1-carboxylate (0.37 g, 90% yield) as the trifluoroacetic acid salt. MS (EI) for C20H25N4O3: 367 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637499B2
Source datasetuspto-grants-2014_01
ORD IDord-a4f610fcec6542d8bf95e9046de86e70
Source noteuspto-grants-2014_01