HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253029Generated: October 31, 2026
Acetyl chloride → HCID 66857789, compound
https://huagongshe.com/reaction/253029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 66857824 | HCID 66857824 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66857789 | HCID 66857789 | — |
Reaction Steps
To a solution of 2-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-6-((3R,5S)-3,5-dimethyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (80 mg, 0.14 mmol) in dichloromethane (5 mL) was added triethylamine (40 μL, 2.0 equivalents) followed by acetyl chloride (15 μL, 1.5 eq.). After stirring overnight, the reaction mixture was diluted with dichloromethane, washed with aqueous sodium carbonate solution, dried (MgSO4) and the solvent removed in vacuo to yield 1-((2R,6S)-4-{2-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl}-2,6-dimethyl-piperazin-1-yl)-ethanone (80 mg) as a white solid. Removal of the tert-butyldimethylsilyl protecting group was performed as described above to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07872003B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-3d7cfe7766e84f399c82d99e452bc7b6 |
|---|
| Source note | uspto-grants-2011_01 |
|---|