HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Chloromethyl)quinoline → HCID 178465626, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Chloromethyl)quinoline | HCID 20394 | — |
| Reactant | HCID 178513185 | HCID 178513185 | — |
| Product | HCID 178465626 | HCID 178465626 | 65% |
Reaction Steps
In a similar manner to Example 1A and using 2-chloromethyl quinoline, 3-(2-quinolinylmethoxy)acetophenone is prepared (13.1 g, m.p. 57°-59° C., 47% yield). This product is reacted with amino guanidine bicarbonate as in 1B above to give 2.35 g of product (65% yield), m.p. 168°-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04889935 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-fd138a62c7684a99a2cd684fab6d1b45 |
| Source note | uspto-grants-1989_12 |