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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77709Generated: October 25, 2026

3-(Trifluoromethyl)phenyl isocyanate → N-[4-Methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)phenyl]-N'-[3-(trifluoromethyl)-phenyl]urea

https://huagongshe.com/reaction/77709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenyl isocyanateHCID 9483—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)anilineHCID 69043120—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-Methyl-3-(9H-pyrimido[4,5-b]indol-6-yl)phenyl]-N'-[3-(trifluoromethyl)-phenyl]ureaHCID 59774725—

Reaction Steps

To 1-isocyanato-3-(trifluoromethyl)benzene (9.8 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 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 (17.1 mg, 46.6%). 1H NMR (300 MHz, DMSO): δ 13.1 (bs, 1H), 9.66 (s, 1H), 9.15 (s, 2H), 8.92 (s, 1H), 8.33 (s, 1H), 8.01 (s, 1H), 7.72 (d, 1H), 7.62 (dd, 1H), 7.4-7.6 (m, 3H), 7.2-7.4 (m, 3H), 2.21 (s, 3H). MS (EI) m/z=462 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841318B2
Source datasetuspto-grants-2014_09
ORD IDord-c38b2953652d47b685573ba2f8d9f2d5
Source noteuspto-grants-2014_09