HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-dimethyl-1H-indol-5-amine → 4(2,3-Dimethylindol-5-ylamino)-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-dimethyl-1H-indol-5-amine | HCID 258688 | — |
| Reactant | 4-Chloro-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline | HCID 11141792 | — |
| Product | 4(2,3-Dimethylindol-5-ylamino)-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline hydrochloride | HCID 22030954 | 76.3% |
Reaction Steps
Using an analogous procedure to that described in Example 37, 4-chloro-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline (100 mg, 0.31 mmol), (prepared as described for the starting material in Example 9), was reacted with 5-amino-2,3-dimethylindole (55 mg, 0.34 mmol) to give 4(2,3-dimethylindol-5-ylamino)-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazoline hydrochloride (114 mg, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074800B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-a64612f1488145b3a1017e0a6b4aac55 |
| Source note | uspto-grants-2006_07 |