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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N1,N1-bis(2-methoxyethyl)-3-methylbutane-1,3-diamine | HCID 64679532 | — |
| Reactant | 8-iodo-3-methyl-2-(methylsulfinyl)quinazolin-4(3H)-one | HCID 89782167 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2((4-(bis(2-methoxyethyl)amino)-2-methylbutan-2-yl)amino)-8-iodo-3-methylquinazolin-4(3H)-one | HCID 89782127 | 183.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394297B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-3f71d11e621148d7b6753e4cbcbbb4d4 |
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| Source note | uspto-grants-2016_07 |
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