HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 118524025, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2S)-2-Methyloxirane | HCID 146262 | — |
| Reactant | HCID 90031248 | HCID 90031248 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 118524025 | HCID 118524025 | 63.7% |
Reaction Steps
Using similar reaction conditions as described in step-ii of example-7, tert-butyl 4-(5-(3-(1-(3-fluorobenzyl)-1H-pyrazol-4-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyrazin-2-yl)piperazine-1-carboxylate (400 mg, 0.56 mmol) was deprotected in HCl in ether (10 ml) to afford crude compound. Using similar reaction conditions as described in Step-i of example-82A, above crude was alkylated using (S)-2-methyloxirane (163 mg, 2.8 mmol), DIPEA (217 mg, 1.68 mmol) and ethanol (10 mL) to get 240 mg (63.7% yield) of the titled compound. MS: m/z=667.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09353107B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-cfe29e59c3b3475cabbb9a32008b8656 |
| Source note | uspto-grants-2016_05 |