HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanimidamide, hydrochloride (1:1) → 6-(3-chloropropoxy)-7-methoxy-1H-quinazolin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanimidamide, hydrochloride (1:1) | HCID 10313058 | — |
| Reactant | Methyl 2-amino-5-(3-chloropropoxy)-4-methoxybenzoate | HCID 23032997 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-(3-chloropropoxy)-7-methoxy-1H-quinazolin-4-one | HCID 178486870 | 76% |
Reaction Steps
In the manner described in Example 16A Step 4, methyl 2-amino-5-(3-chloropropoxy)-4-methoxybenzoate (6.0 g, 21.9 mmol) in EtOAc from the previous step was reacted with formamidine hydrochloride as in Example 16A Step 4 to give 6-(3-chloropropoxy)-4-hydroxy-7-methoxyquinazoline (4.48 g, 16.7 mmol, 76%). 1H NMR (300 MHz, DMSO-d6) δ 12.10 (br s, 1H), 8.00 (s, 1H), 7.47 (s, 1H), 7.15 (s, 1H), 4.19 (t, 2H), 3.97 (s, 3H), 3.81 (t, 2H), 2.27-2.19 (m, 2H); LC-MS (ESI) m/z 269 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09320739B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-c52570bb1cd04d88bfd8a9c2b5d031ad |
| Source note | uspto-grants-2016_04 |