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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055159Generated: November 1, 2026

Toluene → HCID 69116127, compound

https://huagongshe.com/reaction/2055159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
ReactantHCID 69116126HCID 69116126—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69116127HCID 6911612788.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 7.53 mL of a 65% weight toluene solution of sodium bis(2-methoxyethoxy)aluminum hydride (Red-Al, 24.2 mmol) in 90 mL of tetrahydrofuran at 0° C. was added 5.0 g of (3-{4-[3-chloro-4-(6-methyl-pyridin-3-yloxy)-phenylamino]-quinazolin-6-yl}-prop-2-ynyl)-carbamic acid tert-butyl ester as a solid. The reaction was stirred at 0° C. for 2 hours, quenched with 10% aqueous potassium carbonate and extracted with ethyl acetate. The combined organics were dried and evaporated. The crude material was purified on 115 g of silica gel, eluting with 80% ethyl acetate/hexanes to afford 4.42 g of E-(3-{4-[3-chloro-4-(6-methyl-pyridin-3-yloxy)-phenylamino]-quinazolin-6-yl}-allyl)-carbamic acid tert-butyl ester. 1H NMR (CDCl3): δ 8.66 (s, 1), 8.24 (m, 1), 8.03 (m, 2), 7.77-7.65 (m, 3), 7.13 (m, 2), 6.97 (d, J=8.7 Hz, 1), 6.54 (d, 1), 6.35 (m, 1), 4.9 (m, 1), 3.90 (m, 2), 2.52 (s, 3), 1.46 (s, 9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332493B2
Source datasetuspto-grants-2008_02
ORD IDord-666fc27f6d354a2184db4040ac48d88f
Source noteuspto-grants-2008_02