HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518905Generated: October 31, 2026
HCID 86698063, compound → HCID 86698062, compound
https://huagongshe.com/reaction/518905
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86698063 | HCID 86698063 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 86698062 | HCID 86698062 | 50.4% |
Reaction Steps
A solution of 517 mg of the {[6-(hydroxymethyl)-7-(5-fluoro-2-methoxyphenyl)thieno[3,2-d]pyrimidin-2-yl][4-(4-methylpiperazin-1-yl)-2-(propan-2-yloxy)phenyl]amino}methanol mixture in 24 ml of THF and 10 ml of 1M sodium hydroxide is stirred at ambient temperature for 4 h. The mixture is extracted three times with 10 ml of ethyl acetate. The organic phases are washed with 10 ml of water and the organic phases are concentrated under vacuum. The crude product is purified on 80 g of silica, elution being carried out with 5-8% of methanol in dichloromethane, so as to obtain a yellow foam. After trituration with ether, the resulting solid is filtered off and dried under vacuum, so as to obtain 247 mg of [7-(5-fluoro-2-methoxyphenyl)-2-{[4-(4-methylpiperazin-1-yl)-2-(propan-2-yloxy)phenyl]amino}thieno[3,2-d]pyrimidin-6-yl]methanol in the form of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09115140B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-b4ca152ae5884405b55f6cb3b044feb2 |
|---|
| Source note | uspto-grants-2015_08 |
|---|