HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874947Generated: November 1, 2026
Diisopropylethylamine → HCID 59451603, compound
https://huagongshe.com/reaction/1874947
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 3-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile | HCID 59451392 | — |
| Reactant | HCID 68485369 | HCID 68485369 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59451603 | HCID 59451603 | 38% |
Reaction Steps
HATU (0.061 g, 0.161 mmol) was added as a solid to a solution of 3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.050 g, 0.161 mmol), 2,3-dihydro-7H-[1,4]oxathiino[3,2-e]indole-8-carboxylic acid (0.038 g, 0.161 mmol) and DIPEA (0.028 mL, 0.161 mmol) in DMF (1 mL). After 2 hours the reaction mixture was poured into EtOAc and water and the organic layer separated. The organic layer was dried over MgSO4, filtered and the solvent evaporated. The residue was dissolved in MeOH and purification was accomplished by reverse-phase HPLC (water/acetonitrile with 0.1% TFA) to afford the title compound (0.032 g, 38%) as a white solid. 1H NMR (400 MHz, Acetone-d6) δ ppm 10.76 (br. s., 1H), 8.36 (t, 1H), 7.64 (t, 1H), 7.42-7.52 (m, 2H), 7.39-7.42 (m, 2H), 7.20 (dd, 1H), 7.00 (dd, 1H), 6.77 (d, 1H), 4.70 (d, 2H), 4.38-4.43 (m, 2H), 3.23-3.28 (m, 2H). LCMS: m/z=528.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-0e7be59ba38d47de89b95d3da0b7db80 |
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| Source note | uspto-grants-2012_11 |
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