HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602307Generated: October 31, 2026
3,5-Dimethylaniline → HCID 11964856, compound
https://huagongshe.com/reaction/602307
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dimethylaniline | HCID 7949 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57971149 | HCID 57971149 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11964856 | HCID 11964856 | 41% |
Reaction Steps
O-(7-Azabenzotriazole-1-yl)-N,N,N′,N′-tetrauroniumhexafluorophosphate (110 mg, 0.29 mmol) was added to a solution of 2-(2-aminopyrimidin-4-ylmethylthio)nicotinic acid (60 mg, 0.24 mmol, Reference Compound No. 12-1), 3,5-dimethylaniline (33 μL, 0.27 mmol) and N,N-diisopropylethylamine (0.93 μL, 0.53 mmol) in anhydrous N,N-dimethylformamide (1.0 mL) at room temperature, and the mixture was stirred for 18 hours. Ethyl acetate (30 mL) was added thereto, and then the whole was washed with saturated aqueous sodium hydrogencarbonate solution (50 mL) and brine (50 mL), then the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the precipitated solid was filtered off, and washed with 50% diethylether-ethyl acetate solution. The solid was then dried at 60° C. under reduced pressure to give 35 mg of the target compound as a light brown solid (Yield: 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906511B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-c9e54d16ba0c41198ebaff6802d1d479 |
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| Source note | uspto-grants-2011_03 |
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