Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871598Generated: October 27, 2026

Diisopropylethylamine → HCID 58267805, compound

https://huagongshe.com/reaction/871598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPhenyl 3-methoxy-4-(trifluoromethyl)phenylcarbamateHCID 66876321—
Reactant3-(6-Methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)anilineHCID 66876764—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 58267805HCID 58267805—

Reaction Steps

The procedure for Example 138B was used to react phenyl 3-methoxy-4-(trifluoromethyl)phenylcarbamate described in Example 190B (144 mg, 0.46 mmol) with 3-(6-methoxy-7-(2-methoxyethoxy)quinazolin-4-ylthio)aniline described in Example 231A (110 mg, 0.31 mmol). To this solution was added diisopropylethyl amine (80 μL, 0.46 mmol) and DMAP (4.0 mg, 0.03 mmol). The reaction was concentrated to dryness and purified by silica gel chromatography eluting with ethyl acetate/dichloromethane 0-50% over 75 minutes. The main peak collected and concentrated, then triturated with dichloromethane to give a solid weighing 43 mg. 1H (DMSO-d6) 9.19 (s, 1H), 9.04 (s, 1H), 8.70 (s, 1H), 7.84 (s, 1H), 7.6-7.40 (m, 4H), 7.35 (m, 2H), 7.25 (m, 1H), 7.00 (m, 1H), 4.34 (m, 2H), 4.00 (s, 3H), 3.84 (s, 3H), 3.78 (m, 2H). LCMS (ESI) m/z 575 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969587B2
Source datasetuspto-grants-2015_03
ORD IDord-442141300f07447798b03620909e0de0
Source noteuspto-grants-2015_03