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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056358Generated: November 1, 2026

N1,N1-bis(2-methoxyethyl)-3-methylbutane-1,3-diamine → 2((4-(bis(2-methoxyethyl)amino)-2-methylbutan-2-yl)amino)-8-iodo-3-methylquinazolin-4(3H)-one

https://huagongshe.com/reaction/1056358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN1,N1-bis(2-methoxyethyl)-3-methylbutane-1,3-diamineHCID 64679532—
Reactant8-iodo-3-methyl-2-(methylsulfinyl)quinazolin-4(3H)-oneHCID 89782167—
Solventtert-ButanolHCID 6386—
Product2((4-(bis(2-methoxyethyl)amino)-2-methylbutan-2-yl)amino)-8-iodo-3-methylquinazolin-4(3H)-oneHCID 89782127183.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A glass microwave reaction vessel was charged with N1,N1-bis(2-methoxyethyl)-3-methylbutane-1,3-diamine (50 mg, 0.229 mmol) and 8-iodo-3-methyl-2-(methylsulfinyl)quinazolin-4(3H)-one (700b; 80 mg, 0.229 mmol) in tBuOH (0.5 mL). The reaction mixture was stirred and heated in a Initiator microwave reactor (Personal Chemistry, Biotage AB, Inc.) at 120° C. for 45 min. Similarly another two batches (50 mg and 170 mg) were carried out. The three batches were combined and the solvent was removed. The residue was purified with silica gel chromatography (eluted with 0-5% MeOH in DCM) to give 2((4-(bis(2-methoxyethyl)amino)-2-methylbutan-2-yl)amino)-8-iodo-3-methylquinazolin-4(3H)-one (210 mg, 0.42 mmol). MS (ESI, pos. ion) m/z: 503 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394297B2
Source datasetuspto-grants-2016_07
ORD IDord-3f71d11e621148d7b6753e4cbcbbb4d4
Source noteuspto-grants-2016_07