HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 59743406, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 69309534 | HCID 69309534 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 59743406 | HCID 59743406 | 58.3% |
Reaction Steps
A solution of [1-(4-{4-[4-(3-methanesulfonyl-propoxy)-indol-1-yl]-pyrimidin-2-yl-amino}-cyclohexanecarbonyl)-piperidin-4-ylmethyl]-carbamic acid t-butyl ester (0.827 g, 1.236 mM) in 10 mL of 10% HCl soln./EtOH was briefly heated on a steam bath, stirred for 7 hours at RT, concentrated to half volume and cooled in an ice bath. The light yellow solid was collected by filtration, washed with cold EtOH, and dried at 60° C. in vacuo. The product was extracted into DCM, crystallized from EtOH, and dried in vacuo at 60° C. to yield (4-aminomethyl-piperidin-1-yl)-(4-{4-[4-(3-methanesulfonyl-propoxy)-indol-1-yl]-pyrimidin-2-ylamino}-cyclohexyl)-methanone (Compound 304) as a white solid (0.41 g, mp 124-126° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399462B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-ae3f4104bfa44e76a6ac70f50d2b4ded |
| Source note | uspto-grants-2013_03 |