HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Acetoxy-2-bromoethane → 2-Anilino-6-chloro-9-(2-acetoxyethyl)purine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Acetoxy-2-bromoethane | HCID 13564 | — |
| Reactant | 9H-Purin-2-amine, 6-chloro-N-phenyl- | HCID 5271882 | — |
| Product | 2-Anilino-6-chloro-9-(2-acetoxyethyl)purine | HCID 10404476 | 47% |
Reaction Steps
2-Anilino-6-chloropurine was reacted with 2-acetoxyethyl bromide as described above in A.a. 2-Anilino-6-chloro-9-(2-acetoxyethyl)purine was isolated in a 47% yield, mp 193°-194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646155 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-05b8077bbc9e4ef0a0b475677bbeff90 |
| Source note | uspto-grants-1997_07 |