HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756410Generated: October 28, 2026
Sodium → Methyl 4-(3-benzyloxy-6-nitroindazol-1-ylmethyl)-3-methoxybenzoate
https://huagongshe.com/reaction/1756410
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178497911 | HCID 178497911 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-(3-benzyloxy-6-nitroindazol-1-ylmethyl)-3-methoxybenzoate | HCID 23365833 | 120.8% |
Reaction Steps
Methyl 4-(3-hydroxy-6-nitroindazol-1-ylmethyl)-3-methoxybenzoate (T) (35.7 g.) was added to a mixture of sodium (2.3 g.) and methanol (200 ml.). The mixture was stirred for 18 hours, and evaporated. The residue was dissolved in N,N-dimethylformamide (100 ml.) , cooled to 0° C., and benzyl bromide (15.5 ml.) added. After 18 hours at ambient temperature, ethyl acetate and 1N sodium hydroxide solution were added. The precipitate was isolated by filtration, washed with ether, and chromatographed by HPLC on silica gel, eluting with dichloromethane, to give methyl 4-(3-benzyloxy-6-nitroindazol-1-ylmethyl)-3-methoxybenzoate (CC) (27 g., 60%) as a solid; NMR (250 MHz, DMSO-d6): 3.84(s,3H, OMe); 3.86(s,3H, OMe); 5.38(s,2H, NCH2); 5.65(s,2H, OCH2); 6.95(d,1H); 7.36 (m,3H); 7.46(m,5H); 7.86(m,2H); 8.66(s,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05440035 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-d83e72ded03b4d35a9bf5a657233025f |
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| Source note | uspto-grants-1995_08 |
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