HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → HCID 21516636, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | HCID 21516628 | HCID 21516628 | — |
| Product | HCID 21516636 | HCID 21516636 | — |
Reaction Steps
Reaction of acrylonitrile with 3-hydroxy-3-(m-tolyl)indolin- 2-one by a procedure analogous to that of Example 1 gives 1-(2-cyanoethyl)- 3-hydroxy-3-(m-tolyl)indole- 2-one. Hydrogenation of 1-(2-cyanoethyl)-3-hydroxy-3-(m-tolyl) indolin-2-one by a procedure analogous to that of Example 2 gives 1-(3-aminopropyl)-3-hydroxy-3-(m-tolyl)indolin- 2-one. Cyclodehydration of 1-(3-aminopropyl)-3-hydroxy-3-(m-tolyl) indolin -2-one by a procedure analogous to that of Example 3 gives 2,3,4,10-tetrahydro-10-(m-tolyl) pyrimido[ 1,2-a] indol-10-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976645 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-146df67ae474479f8d6f7627fd229cdd |
| Source note | uspto-grants-1976_08 |