HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239781Generated: October 31, 2026
2-Furancarboxylic acid, hydrazide → furan-2-carboxylic acid N'-{2-amino-7-[2-(t-butyldimethylsilanyloxy)ethyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}-hydrazide
https://huagongshe.com/reaction/2239781
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Furancarboxylic acid, hydrazide | HCID 18731 | — |
| Reactant | 7-[2-(t-butyldimethylsilanyloxy)ethyl]-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine | HCID 86623463 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | furan-2-carboxylic acid N'-{2-amino-7-[2-(t-butyldimethylsilanyloxy)ethyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}-hydrazide | HCID 68414130 | — |
Reaction Steps
The title A compound, 7-[2-(t-Butyldimethylsilanyloxy)ethyl]-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine (100 mg, 0.3 mmol) and 2-furoic acid hydrazide (76 mg, 0.6 mmol) are taken into 3 mL of n-butanol. The mixture is stirred at 120° C. under N2 for 2 h. The solvent is evaporated under vacuum and the residue is purified by flash chromatography using EtOAc/MeOH (95/5) as eluent to give furan-2-carboxylic acid N′-{2-amino-7-[2-(t-butyldimethylsilanyloxy)ethyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}-hydrazide: LC/MS (M+1=417). 1H NMR (CDCl3, 400 MHz) δ-0.08 (s, 6H), 0.84 (s, 9H), 3.85 (t, 2H, J=4.8 Hz), 4.12 (t, 2H, J =4.8 Hz), 4.81 (br s, 2H, NH2), 6.26 (d, 1H, J=2.4 Hz), 6.51 (m, 1H), 6.74 (d, 1H, J=2.4 Hz), 7.20 (d, 1H, J=2.8 Hz), 7.27 (d, 1H, J=2.8 Hz), 7.49 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723343B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-75a28725d1944eea8ece51fc2e4314d2 |
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| Source note | uspto-grants-2010_05 |
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