HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-(-)-1-Phenylethyl isocyanate → 1-[6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazolin-4-yl]-3-[(S)-(-)-alpha-methylbenzyl]urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-(-)-1-Phenylethyl isocyanate | HCID 2724173 | — |
| Reactant | 4-amino-6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazoline | HCID 22243908 | — |
| Product | 1-[6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazolin-4-yl]-3-[(S)-(-)-alpha-methylbenzyl]urea | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06806274B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-70abe2ef17b44d0ab0a81fbfc16281cf |
| Source note | uspto-grants-2004_10 |