HuagongsheHuagongshe Chemistry Print Report · For research reference only
1423057-50-4 → HCID 178420284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1423057-50-4 | HCID 136227344 | — |
| Reactant | HCID 136341309 | HCID 136341309 | — |
| Product | HCID 178420284 | HCID 178420284 | 16% |
| Product | HCID 178420285 | HCID 178420285 | 11% |
Reaction Steps
The reactions in Synthetic Examplea 134 were carried out in substantially the same manners except that N-phenethyl-4-(7H-pyrrolo[3,2-e][1,2,3]triazolo[1,5-c]pyrimidin-1-yl)cyclohexanamine obtained in Synthetic Examplea 123 was used instead of 4-{[4-(7H-pyrrolo[3,2-e][1,2,3]triazolo[1,5-c]pyrimidin-1-yl)cyclohexyl]amino}benzonitrile to give cis-N-phenethyl-4-(7H-pyrrolo[3,2-e][1,2,3]triazolo[1,5-c]pyrimidin-1-yl)cyclohexanamine (Synthetic Examplea 135a; colorless solid, 3.22 mg, yield 16%) in a less polar fraction and trans-N-phenethyl-4-(7H-pyrrolo[3,2-e][1,2,3]triazolo[1,5-c]pyrimidin-1-yl)cyclohexanamine (Synthetic Examplea 135b; colorless solid, 2.52 mg, yield 11%) in a more polar fraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216999B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-b18467f4753248dc893193108487156e |
| Source note | uspto-grants-2015_12 |