Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57812413 | HCID 57812413 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57812621 | HCID 57812621 | — |
Reaction Steps
3-(1-Azetidin-3-yl-1,2,3,6-tetrahydropyridin-4-yl)-7-[(R)-1-(2,6-dichloro-3-fluoro-phenyl)ethoxy]furo[3,2-c]pyridin-6-ylamine (10.0 mg, 0.0209 mmol), trimethylsilyl isocyanate (4.25 μL, 0.0314 mmol), DMF (1.0 mL, 13 mmol) and DIPEA (7.30 μL, 0.0419 mmol) were mixed together and stirred at room temperature for 1 hour. The crude was passed through SCX-2 SPE and the product was release by 2 M NH3 in methanol for MDP purification. MS (ES+): m/z 555.05/557.04 (100/76) [MH+]. HPLC: tR=0.55 min (HPLC-ACQUITY, Analytical). 1H NMR (400 MHz, CD3OD): δ=1.88 (d, J=6.8 Hz, 3H), 2.56 (br. s., 2H), 2.67-2.73 (m, 2H), 3.15-3.22 (m, 2H), 3.34-3.42 (m, 1H), 3.89 (dd, J=8.6, 5.3 Hz, 2H), 4.01-4.09 (m, 2H), 6.27 (br. s., 1H), 6.50 (q, J=6.7 Hz, 1H), 7.21 (t, J=8.6 Hz, 1H), 7.40 (dd, J=9.0, 4.9 Hz, 1H), 7.63 (s, 1H), 8.19 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022206B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-8811d704c4b04e2a995e03fa3025c617 |
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| Source note | uspto-grants-2011_09 |
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