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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506173Generated: October 31, 2026

1423057-50-4 → HCID 178420284, compound

https://huagongshe.com/reaction/1506173

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1423057-50-4HCID 136227344—
ReactantHCID 136341309HCID 136341309—
ProductHCID 178420284HCID 17842028416%
ProductHCID 178420285HCID 17842028511%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-b18467f4753248dc893193108487156e
Source noteuspto-grants-2015_12