Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (3R)-N-((1R)-1-((4-Chlorophenyl)methyl)-2-(4-cyclohexyl-4-(1H-1,2,4-triazol-1-ylmethyl)-1-piperidinyl)-2-oxoethyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxamide | HCID 9938402 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131726277 | HCID 131726277 | 59% |
Reaction Steps
resin 2 (0.65 mmol g−1 (est.), 1.49 g) in dry DCM (25 cm3) were treated with PBr3 (2.28 mmol, 216 mm3) at 20° C. for 12 h. The resin was filtered off, washed with DCM (200 cm3), dried at air and transferred to a flask with DMF (20 cm3) and THIQ (5.7 mmol, 725 mm3) was added. The resin was stirred at r.t. for 24 h, washed with DMF, MeOH, DCM, and MeOH. It was dried under high vacuum. 1.45 g (0.5 mmol g−1 (est.)) of it was resuspended in DMF (10 cm3) and allyl bromide (150 mm3, 1.7 mmol) was added. After 5 d at 20° C. the solid was filtered off, washed with DMF (100 cm3) and DCM (100 cm3). The resin was then treated with DIPEA (1.00 mmol, 175 mm3) in DCM (25 cm3). After 2 days the solid material was filtered off and washed with DCM and MeOH. Yield of resin 3 1.28 g (max. est. yield: 1.25 g). The solvent was removed from the filtrate and gave analytical pure 4 (0.47 mmol, 120 mg, 59%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183367B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-9509a590137e498dae6fd5594241a132 |
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| Source note | uspto-grants-2007_02 |
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