Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (1R,4S)-4-Amino-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 86686674 | — |
| Reactant | HCID 117728791 | HCID 117728791 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 117729017 | HCID 117729017 | 19% |
Reaction Steps
A suspension of sodium hydride (60% dispersion in oil, 56 mg, 1.39 mmol) in dry DMF (2.0 mL) under nitrogen was treated with Intermediate 1 (46 mg, 0.28 mmol) and the mixture was stirred for 20 min. Intermediate 13d (110 mg, 0.28 mmol) was added and the mixture was heated to 60° C. for 1.75 h then quenched with MeOH. The mixture was further diluted with MeOH and applied to a pre-conditioned (MeOH) SCX-2 cartridge (10g). The cartridge was eluted with MeOH then 2M NH3 in MeOH. The relevant fractions were combined and concentrated in vacuo. The residue was dissolved in DCM containing a few drops of MeOH and purified by FCC, using 0-10% [2M NH3 in MeOH] in DCM, to give the title compound (28 mg, 19%). LCMS (Method 3): Rt 2.08 min, m/z 537, 539 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359354B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-86fe9426aef54eccb0785303799f0a8c |
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| Source note | uspto-grants-2016_06 |
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