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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871561Generated: October 29, 2026

Diisopropylethylamine → HCID 58267923, compound

https://huagongshe.com/reaction/871561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(6,7-Dimethoxyquinazolin-4-ylthio)anilineHCID 56953627—
Reactantphenyl 1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-ylcarbamateHCID 59394502—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58267923HCID 5826792317%

Reaction Steps

Using the procedure described in Example 159B, phenyl 1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-ylcarbamate described in Example 165A (0.114 g, 0.4 mmol) was reacted with 3-(6,7-dimethoxyquinazolin-4-ylthio)aniline from Example 115B (0.125 g, 0.4 mmol), and N,N-diisopropylethylamine (0.5 mL) in THF (6 mL) at 50° C. for 3 hours, to afford 1-[3-(6,7-dimethoxyquinazolin-4-ylthio)phenyl]-3-[1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl]urea as solid (0.035 g, 17%). 1H NMR (300 MHz, CDCl3) δ 9.43 (br, 1H), 8.77 (s, 1H), 7.80 (m, 1H), 7.63 (d, 1H), 7.44 (t, 1H), 7.38 (m, 2H), 7.28 (s, 1H), 7.20 (s, 1H), 6.31 (s, 1H), 4.08 (s, 3H), 4.06 (s, 3H), 3.91 (s, 3H); LC-MS (ESI) m/z 505 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969587B2
Source datasetuspto-grants-2015_03
ORD IDord-555f03d2dbc84ac8902669bfe592b85b
Source noteuspto-grants-2015_03