HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502498Generated: October 31, 2026
(Diethylamino)sulfur trifluoride → HCID 58008750, compound
https://huagongshe.com/reaction/1502498
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | HCID 58008593 | HCID 58008593 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58008750 | HCID 58008750 | 20% |
Reaction Steps
To a stirred suspension of 3-((4-amino-3-(hydroxymethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-8-methyl-2-o-tolylisoquinolin-1(2H)-one (compound 4503) (50 mg, 0.12 mmol) in anhydrous DCM (2 mL) at 0° C. under an argon atmosphere, diethylaminosulfur trifluoride (DAST, 77 μL, 0.59 mmol) was slowly added and the resulting mixture was stirred from 0° C. to room temperature for 5 h. The reaction was quenched with water and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by prep-TLC plate (7% MeOH/DCM) to afford the desired product, 3-((4-amino-3-(fluoromethyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-8-methyl-2-o-tolylisoquinolin-1(2H)-one (4504, compound 310 in Table 4) (10.3 mg, 20% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206182B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-34d64a82c71041f4970157da9d159bc6 |
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| Source note | uspto-grants-2015_12 |
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