HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921725Generated: October 31, 2026
(2S)-2-Methyloxirane → HCID 86708606, compound
https://huagongshe.com/reaction/921725
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2S)-2-Methyloxirane | HCID 146262 | — |
| Reactant | HCID 86708607 | HCID 86708607 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 86708606 | HCID 86708606 | 32.9% |
Reaction Steps
A suspension of 2-((3-(azetidin-3-yl)-2-chloro-5-cyanophenyl)amino)-4-(ethylamino)imidazo[2,1-f][1,2,4]triazine-7-carbonitrile (Example 367)(16 mg, 0.041 mmol) and (S)-(−)-propylene oxide (0.085 mL, 1.22 mmol) in a mixture of NMP (0.8 mL) and MeOH (0.2 mL) was stirred at 50° C. for 4.5 hr. The solvent was removed and the product was purified by preparative HPLC (Waters XBridge C18, 19×200 mm, 5-μm particles; Mobile Phase A: water with 20-mM ammonium acetate; Mobile Phase B: 95:5 acetonitrile: water with 20-mM ammonium acetate; Gradient: 15-55% B over 20 minutes, then a 5-minute hold at 100% B; Flow: 20 mL/min) to give the title compound (6.1 mg). This was converted to the mono HCl salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273057B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-ca3cf582faa04b27bafb7bf512a1fadf |
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| Source note | uspto-grants-2016_03 |
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