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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474927Generated: October 30, 2026

Hydrochloric Acid → HCID 66873989, compound

https://huagongshe.com/reaction/474927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 70805202HCID 70805202—
SolventMethanolHCID 887—
ProductHCID 66873989HCID 6687398951%

Reaction Steps

tert-Butyl 8-(2-oxo-4-(5-(trifluoromethyl)pyridin-2-yl)pyridin-1(2H)-yl)-3,4,5,6-tetrahydroazepino[4,3-b]indole-2(1H)-carboxylate (30 mg, 0.057 mmol) was treated with 1.25 M HCl in MeOH (5.5 mL), and the resulting solution was stirred at ambient temperature for 18 h. The solution was partially concentrated and diluted with Et2O. The resulting solids were collected by filtration, washed with Et2O and dried to yield the title compound (13 mg, 51%) as a yellow powder: mp 310-320° C. decomp.; 1H NMR (500 MHz, DMSO-d6) δ 11.51 (s, 1H), 9.14 (s, 1H), 8.81 (s, 2H), 8.39 (dd, J=8.5, 2.0 Hz, 1H), 8.34 (d, J=8.5 Hz, 1H), 7.82 (d, J=7.5 Hz, 1H), 7.67 (d, J=8.5 Hz, 1H), 7.41 (d, J=2.0 Hz, 1H), 7.26 (d, J=2.0 Hz, 1H), 7.08-7.04 (m, 2H), 4.44 (s, 2H), 3.49-3.47 (m, 2H), 3.06-3.04 (m, 2H), 2.03-2.01 (m, 2H); ESI MS m/z 425 [M+H]+; HPLC (Method A) 96.9% (AUC), tR=13.7 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637501B2
Source datasetuspto-grants-2014_01
ORD IDord-bc63e40c9b4b4817a822b9854d830636
Source noteuspto-grants-2014_01