HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Benzodioxol-5-amine → 4-Quinazolinamine, N-1,3-benzodioxol-5-yl-2-chloro-N-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Benzodioxol-5-amine | HCID 84310 | — |
| Reactant | 2,4-Dichloroquinazoline | HCID 252886 | — |
| Reactant | N-(2H-1,3-Benzodioxol-5-yl)-2-chloroquinazolin-4-amine | HCID 22692858 | — |
| Product | 4-Quinazolinamine, N-1,3-benzodioxol-5-yl-2-chloro-N-methyl- | HCID 11536924 | — |
Reaction Steps
(2-Chloro-quinazolin-4-yl)-(3,4-methylenedioxyphenyl)-amine: The title compound was prepared from 3,4-methylenedioxyphenylamine and 2,4-dichloroquinazoline by a procedure similar to example 1b and was isolated as solids (45% yield). 1H NMR (CDCl3): 7.81-7.83 (m, 3H), 7.51-7.56 (m, 2H), 7.44 (d, 1H, J=2.1), 6.98 (dd, 1H, J=2.1, 8.1), 6.82 (d, 1H, J=8.1), 6.01 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258145B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-e7cf8aa7c678440a93eceb064d015318 |
| Source note | uspto-grants-2012_09 |