Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21894791 | HCID 21894791 | — |
| Reactant | HCID 59380394 | HCID 59380394 | — |
| Product | HCID 59380419 | HCID 59380419 | — |
Reaction Steps
To a solution of 4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)[1]benzothieno[2,3-d]pyrimidin-7-ol (150 mg, 0.33 mmol) in EtOH (15 mL) was added (2,3-epoxypropyl)phthalimide (101.2 mg, 0.50 mmol, 1.5 equiv) and triethylamine (1.68 mg, 0.02 mmol, 0.05 equiv) under nitrogen. The reaction mixture was stirred at 80° C. for 15 h and then cooled to rt. The resulting mixture was concentrated in vacuo. The crude material (216 mg, 0.33 mmol) was directly used in the next step without further purification, LCMS RT=3.89 min, [M+H]+=655.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750017B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-6d136a12233d4a66a65ee83ece02758d |
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| Source note | uspto-grants-2010_07 |
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