Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | HCID 68668848 | HCID 68668848 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54583358 | HCID 54583358 | — |
Reaction Steps
To a solution of 8-[5-((S)-2-benzyloxymethyl-4-methyl-piperazin-1-yl)-2-trifluoromethoxy-phenylamino]-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide (53 mg, 0.08 mmol) in DCM (1.7 mL) under an atmosphere of N2, at −78° C. 1M BCl3 in DCM (0.17 mL) was added dropwise. Under complete addition the solution was stirred at 0° C. for 30 min and at room temperature overnight. Then 2 mL of MeOH was added. The solvent was removed under reduced pressure and the residue was diluted with Et2O and decanted to give the desired compound in quantitative yield (46 mg) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614220B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-40282f6a925d4fc699ba8e11c5ca839f |
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| Source note | uspto-grants-2013_12 |
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