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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393240Generated: October 26, 2026

(S)-(-)-1-Phenylethyl isocyanate → 1-[6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazolin-4-yl]-3-[(S)-(-)-alpha-methylbenzyl]urea

https://huagongshe.com/reaction/393240

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(-)-1-Phenylethyl isocyanateHCID 2724173—
Reactant4-amino-6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazolineHCID 22243908—
Product1-[6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazolin-4-yl]-3-[(S)-(-)-alpha-methylbenzyl]ureaHCID 69464186—

Reaction Steps

Using an analogous procedure to that described in Example 14, (S)-(−)-α-methylbenzyl isocyanate was reacted with 4-amino-6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazoline to give the title compound; NMR Spectrum: (CDCl3) 1.4-1.56 (m, 2H), 1.61 (d, 3H), 1.84-2.05 (m, 5H), 2.31 (s, 3H), 2.91 (d, 2H), 3.88 (s, 3H), 4.04 (d, 2H), 5.2 (m, 1H), 7.23 (d, 2H), 7.3-7.41 (m, 5H), 8.66 (s, 1H), 8.7 (s, 1H), 10.58 (s, 1H); Mass Spectrum: M+H+ 450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806274B1
Source datasetuspto-grants-2004_10
ORD IDord-70abe2ef17b44d0ab0a81fbfc16281cf
Source noteuspto-grants-2004_10