HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylaminoethanol → 2-Chloro-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylaminoethanol | HCID 5247031 | — |
| Reactant | 2-Chloro-4-[(5-fluoroquinazolin-4-yl)amino]phenol | HCID 57444978 | — |
| Reactant | 2-Methyl-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenol | HCID 69054007 | — |
| Product | 2-Chloro-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenol | HCID 69057590 | 96% |
Reaction Steps
2-Chloro-4-[(5-fluoroquinazolin-4-yl)amino]phenol was reacted with N-methylaminoethanol using an analogous process to that described in Example 3 for the preparation of 2-methyl-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenol, to give 2-Chloro-4-({5-[2-(methylamino)ethoxy]quinazolin-4-yl}amino)phenol in 96% yield; NMR spectrum (DMSO-d6) 2.41 (s, 3H), 3.05 (t, 2H), 4.36 (t, 2H), 6.97 (d, 1H), 7.12 (d, 1H), 7.31 (d, 1H), 7.63 (1H, dd), 7.70 (t, 1H), 7.96 (s, 1H), 8.47 (s, 1H) 10.47 (bs, 1H); Mass spectrum MH+ 345.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07625908B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-fcbbf74f408b4a1aa969c19ee50c22e2 |
| Source note | uspto-grants-2009_12 |