HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602466Generated: November 1, 2026
Diethyl cyanophosphonate → 1-tert-Butyl 2-methyl (2S,4S)-4-{[(1-isopropyl-1H-indazol-3-yl)carbonyl]amino}pyrrolidine-1,2-dicarboxylate
https://huagongshe.com/reaction/602466
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2S,4S)-1-Tert-butyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate | HCID 5200425 | — |
| Reactant | 1-Isopropyl-1H-indazole-3-carboxylic acid | HCID 10679695 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-tert-Butyl 2-methyl (2S,4S)-4-{[(1-isopropyl-1H-indazol-3-yl)carbonyl]amino}pyrrolidine-1,2-dicarboxylate | HCID 86624149 | 98% |
Reaction Steps
To a stirred solution of 1-isopropyl-1H-indazole-3-carboxylic acid (300 mg, 1.47 mmol) and 1-tert-butyl 2-methyl (2S,4S)-4-aminopyrrolidine-1,2-dicarboxylate (396 mg, 1.62 mmol, Bioorg. Med. Chem., 2002, 10, 1399-1415) in N,N-dimethylformamide (15 mL) were added diethyl cyanophosphonate (0.27 mL, 1.76 mmol) and N,N-diisopropylethylamine (0.31 mL, 1.76 mmol) at room temperature. The resulting mixture was stirred for 14 h at the same temperature and concentrated under reduced pressure. The resulting residue was diluted with ethyl acetate (200 mL), and the solution was washed with water (50 mL×2), brine (50 mL), dried over sodium sulfate, and concentrated under reduced pressure. The resulting residue was chromatographed on a column of silica gel eluting with n-hexane/ethyl acetate (3:1) to give 618 mg (98%) of the title compound as a white amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906532B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-0e325bb512014c9ca763594c0fc0de23 |
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| Source note | uspto-grants-2011_03 |
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