HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 136341325, compound → HCID 178457499, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 136341325 | HCID 136341325 | — |
| Reactant | HCID 136341330 | HCID 136341330 | — |
| Product | HCID 178457498 | HCID 178457498 | 7% |
| Product | HCID 178457499 | HCID 178457499 | 19% |
Reaction Steps
The reactions in Synthetic Examplea 435 were carried out in substantially the same manners except that 2-[4-(7H-pyrrolo[3,2-e][1,2,3]triazolo[1,5-c]pyrimidin-1-yl)cyclohexylidene]propanenitrile obtained in Synthetic Examplea 437 was used instead of 2-[4-(7H-pyrrolo[3,2-e][1,2,3]triazolo[1,5-c]pyrimidin-1-yl)cyclohexylidene]acetonitrile to give 2-[cis-4-(7H-pyrrolo[3,2-e][1,2,3]triazolo[1,5-c]pyrimidin-1-yl)cyclohexyl]propanenitrile (Synthetic Examplea 439a; colorless solid, 0.750 mg, yield 7%) in a less polar fraction and 2-[trans-4-(7H-pyrrolo[3,2-e][1,2,3]triazolo[1,5-c]pyrimidin-1-yl)cyclohexyl]propanenitrile (Synthetic Examplea 439b; colorless solid, 2.00 mg, yield 19%) 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-444503b9b7bb47cb9da605f343f5d1d4 |
| Source note | uspto-grants-2015_12 |