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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894879Generated: October 25, 2026

Diisopropylethylamine → 4-Methoxy-N-[4-methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)phenyl]-3-(trifluoromethyl)-benzamide

https://huagongshe.com/reaction/1894879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Methoxy-3-(trifluoromethyl)benzoyl chlorideHCID 2775298—
Reactant4-methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)anilineHCID 69043120—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-N-[4-methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)phenyl]-3-(trifluoromethyl)-benzamideHCID 59774726—

Reaction Steps

To 4-methoxy-3-(trifluoromethyl)benzoyl chloride (11.0 μL, 0.070 mmol) was added a solution of 4-methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)aniline (17.5 mg, 0.064 mmol) and DIPEA (16 μL, 0.089 mmol) in tetrahydrofuran (THF) (0.4 mL). The reaction was stirred at ambient temperature until LCMS indicated complete reaction, typically 16 hours. The reaction mixture was diluted to a total of 2 mL with THF and MeOH and purified by preparative LCMS to recover the product as a TFA salt (18.6 mg, 49.4%). 1H NMR (300 MHz, DMSO): δ 13.0 (bs, 1H), 10.33 (s, 1H), 9.64 (s, 1H), 9.13 (s, 1H), 8.35 (s, 1H), 8.24 (m, 2H), 7.7-7.8 (m, 3H), 7.63 (dd, 1H), 7.41 (d, 1H), 7.32 (d, 1H), 2.25 (s, 3H). MS (EI) m/z=477 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513270B2
Source datasetuspto-grants-2013_08
ORD IDord-6bfb015e0a7a47f0b0ca9b1b7934a650
Source noteuspto-grants-2013_08