HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Thienylmethyl)amine → 2-Amino-3-cyano-4-thenylaminoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Thienylmethyl)amine | HCID 34005 | — |
| Reactant | 2-Amino-3-cyano4-chloroquinoline | HCID 11481121 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-3-cyano-4-thenylaminoquinoline | HCID 22273720 | — |
Reaction Steps
5 g of 2-amino-3-cyano4-chloroquinoline, prepared as described in Example 1, is stirred with 11 ml of 2-thienylmethylamine at 130° C. for 3 hours. The reaction mixture is poured onto 50 ml of water, the resulting precipitate is filtered off, washed with 50 ml of water. The pale yellow material is recrystallized from 25 ml of ethanol to obtain 5.2 g of title compound, mp.: 208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06969723B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-dfc57241a00742a0b96b530dcc4e6038 |
| Source note | uspto-grants-2005_11 |