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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474952Generated: October 30, 2026

Hydrochloric Acid → HCID 66874864, compound

https://huagongshe.com/reaction/474952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 66873656HCID 66873656—
SolventDichloromethaneHCID 6344—
ProductHCID 66874864HCID 6687486494%

Reaction Steps

To a solution of tert-butyl 6-methyl-8-(2-oxo-4-(6-(trifluoromethyl)pyridin-3-yl)pyrimidin-1(2H)-yl)-1,2,4,5-tetrahydroazepino[4,5-b]indole-3(6H)-carboxylate (36 mg, 0.067 mmol) in dichloromethane (1.0 mL) was added HCl (2M in diethyl ether, 5.0 mL). The resulting slurry was stirred at room temperature for 14 h and then concentrated under reduced pressure. The resulting residue was purified by semi-preparative HPLC (Phenomenex Luna C18 (2), 250.0×21.20 mm, 10 micron, H2O with 0.05% TFA and CH3CN with 0.05% TFA). The clean fractions were combined, concentrated under reduced pressure and lypholized overnight. The trifluroacetate salt was dissolved in a 1:2 mixture of acetonitrile and water (10 mL) and passed through a plug of SAX column. The column was further washed with a 1:2 mixture of acetonitrile and water (10 mL). The combined filtrate was lypholized to give the title compound (30.1 mg, 94%) as a yellow solid: 1H NMR (500 MHz, CD3OD) δ 9.48 (s, 1H), 8.80 (d, J=8.5 Hz, 1H), 8.38 (d, J=6.5 Hz, 1H), 8.02 (d, J=8.0 Hz, 1H), 7.66 (d, J=8.5 Hz, 1H), 7.59 (d, J=1.0 Hz, 1H), 7.36 (d, J=7.0 Hz, 1H), 7.18 (dd, J=8.5, 1.5 Hz, 1H), 3.78 (s, 3H), 3.56 (t, J=5.5 Hz, 2H), 3.50 (t, J=5.5 Hz, 2H), 3.37 (t, J=5.5 Hz, 2H), 3.26 (t, J=5.5 Hz, 2H); ESI MS m/z 440 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637501B2
Source datasetuspto-grants-2014_01
ORD IDord-734bbabbd91a43f7a7d16b10dba92676
Source noteuspto-grants-2014_01