HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775178Generated: October 30, 2026
N-methyl-2-pyrrolidone → HCID 57389786, compound
https://huagongshe.com/reaction/1775178
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Pyridinemethanamine | HCID 19509 | — |
| Reactant | HCID 57963219 | HCID 57963219 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 57389786 | HCID 57389786 | — |
Reaction Steps
In a microwave vial, 7-benzenesulfonyl-5-(2-methanesulfonyl-pyrimidin-5-ylmethyl)-7H-pyrrolo[2,3-d]pyrimidine (58, 12 mg, 0.028 mmol) was mixed with 600 μL of N-methylpyrrolidone and C-pyridin-2-yl-methylamine (59, 19.5 mg, 0.18 mmol). The reaction was irradiated at 160° C. for 40 minutes in microwave, then potassium hydroxide (500 μL, 4.00 M in water) was added and the reaction irradiated at 90° C. for 10 minutes in microwave. The reaction was neutralized with the addition of 120 μL of acetic acid, solvents were removed under vacuum, and the resulting material was dissolved in 400 μL of dimethylsulfoxide for purification by HPLC. Samples were purified on Phenomenex C18 column (50 mm×10 mm ID) with mobile phase A of 0.1% trifluoroacetic acid in water, mobile phase B of 0.1% trifluoroacetic acid in acetonitrile, 20-100% B over 16 minutes at a flow rate of 6 mL/min. Appropriate fractions were collected and solvents removed under vacuum to provide the desired compound. MS (ESI) [M+H+]+=317.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260437B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-47728106b69942e4aa7684416c2e9133 |
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| Source note | uspto-grants-2016_02 |
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