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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917959Generated: November 3, 2026

Diisopropylethylamine → HCID 44242858, compound

https://huagongshe.com/reaction/1917959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(6,7-Dimethoxyquinazolin-4-ylthio)anilineHCID 56953627—
ReactantHCID 66876404HCID 66876404—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 44242858HCID 44242858—

Reaction Steps

The procedure described in Example 138B was used to react phenyl 3-(morpholinomethyl)-5-(trifluoromethyl)phenylcarbamate described in example 151A (140 mg, 0.37 mmol) with 3-(6,7-dimethoxyquinazolin-4-ylthio)aniline from Example 115B (77 mg, 0.25 mmol). To this solution was added diisopropylethyl amine (64 μL, 0.37 mmol) and DMAP (3.0 mg, 0.03 mmol). The reaction was concentrated to dryness and triturated with methanol to give 47 mg. 1H NMR (300 MHz, DMSO-d6) δ 9.15 (s, 1H), 8.98 (s, 1H), 8.70 (s, 1H), 7.88 (d, 2H), 7.55 (m, 2H), 7.44 (m, 1H), 7.35 (s, 2H), 7.25 (m, 2H), 4.00 (s, 6H), 3.58 (s, 4H), 3.34 (s, 2H), 2.39 (s, 4H). LCMS (ESI) m/z 600 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-ad1e55ab344948a898c183eff894aaff
Source noteuspto-grants-2013_12