HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805861Generated: November 3, 2026
N-methyl-2-pyrrolidone → HCID 11962294, compound
https://huagongshe.com/reaction/1805861
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 57693589 | HCID 57693589 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11962294 | HCID 11962294 | 80% |
Reaction Steps
A stirred suspension of NaH (63.8 mg, 2.66 mmol) in dry NMP (1.5 mL) was added 4-aminobenzylnitrile (188 mg, 2.66 mmol) and stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-2-fluoro-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidine (115 mg, 0.32 mmol) in dry NMP (1.7 mL) and stirred at room temperature for 2 h. After completion of the reaction, the resulting mixture was diluted with water and washed with EtOAc 3 times. The combined organic layers were washed with water, NH4Cl, water×2, and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with 1% MeOH:CH2Cl2, which afforded the product as a tan solid (120 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354532B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-d5e0925bc6234d9eb3b6b394c136c08e |
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| Source note | uspto-grants-2013_01 |
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