HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406586Generated: October 31, 2026
Diisopropylethylamine → HCID 59272930, compound
https://huagongshe.com/reaction/1406586
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 2,2-Difluoropropionic acid | HCID 2782825 | — |
| Reactant | HCID 59272916 | HCID 59272916 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59272930 | HCID 59272930 | — |
Reaction Steps
Isobutyl 3-(5-((1R,2S)-2-amino-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propoxy)-1H-indazol-1-yl)benzoate (Mb) (0.5 g, 1.00 mmol), 2,2-difluoropropanoic acid (0.16 g, 1.45 mmol) and HBTU (0.567 g, 1.50 mmol) in DCM (4 mL) was treated with DIEA (0.696 mL, 3.99 mmol), the mixture was stirred at ambient temperature for 1 hour. The reaction was quenched by addition 10% NaHSO4(aq), brine was added to help phase separation. The lower red DCM phase was separated, the waterphase was extracted with one portion of EtOAc, the combined organic solutions were dried over MgSO4 and filtered, solvents was removed by evaporation. Obtained a crude product as red oil. The crude material was further purified by flash chromatography using an 70 g prepacked silica column, an gradient of 0% to 50% EtOAc in Heptane was applied. Fractions with product was combined and solvents was removed by evaporation. An slightly yellow sticky oil was obtained after final evaporation from DCM. Yield 540 mg (91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916600B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-467b859bc55041d4b3ad74a29dd77239 |
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| Source note | uspto-grants-2014_12 |
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