HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205624Generated: November 2, 2026
Diisopropylethylamine → HCID 118214760, compound
https://huagongshe.com/reaction/2205624
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-4-chloro-6-methyl-5-pyrimidinecarbonitrile | HCID 75412446 | — |
| Reactant | HCID 118214761 | HCID 118214761 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 118214760 | HCID 118214760 | — |
Reaction Steps
To crude tert-butyl (S)-4-((5-(1-aminoethyl)-1-methyl-1H-pyrrolo[3,2-b]pyridin-6-yl)amino)piperidine-1-carboxylate was added HOAc (2 drops), followed by ACN (2 mL), 2-amino-4-chloro-6-methylpyrimidine-5-carbonitrile (0.083 g, 0.493 mmol), and DIPEA (0.344 mL, 1.970 mmol). The reaction mixture was stirred at 75° C. for 1 hour. LCMS showed the reaction was complete, though messy. The volatiles were removed by N2 flow. The crude title compound was used without further purification. ESI-MS m/z [M+H]+ calc'd for C26H35N9O2, 506. found 506.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09371321B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-2437996c2afe498ea11bb6a6078700d4 |
|---|
| Source note | uspto-grants-2016_06 |
|---|