HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365209Generated: October 31, 2026
Water → 1-Phenoxy-3-[2-(5-methylindazol-4-ylamino)-ethylamino]-propan-2-ol benzoate
https://huagongshe.com/reaction/365209
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phenyl glycidyl ether | HCID 31217 | — |
| Reactant | 5-Methyl-4-(2-aminoethylamino)-indazole | HCID 20237848 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Phenoxy-3-[2-(5-methylindazol-4-ylamino)-ethylamino]-propan-2-ol benzoate | HCID 53840335 | — |
Reaction Steps
3.0 g Phenyl glycidyl ether and 6.0 g 5-methyl-4-(2-aminoethylamino)-indazole are dissolved in 12 ml. dimethylformamide and left to stand for 2 days at ambient temperature. The reaction mixture is taken up in a little methylene chloride, shaken out three times with a 10-fold amount of water and the methylene chloride solution is dried and separated column chromatographically on silica gel using, as elution agent, methylene chloride-methanol-triethylamine (100:10:1 v/v/v). By evaporation of the pure fractions, there are obtained 5.2 g. of a dark oil, which is dissolved in a little ethyl acetate, mixed with 2.5 g. benzoic acid, filtered off with suction and recrystallized from ethyl acetate, with the use of active charcoal and fullers' earth. There are obtained 3.3 g. (36% of theory) of the desired product in the form of colorless crystals; m.p. 97°-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04608383 |
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| Source dataset | uspto-grants-1986_08 |
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| ORD ID | ord-6bf3dbf10aa94a418705d8dbee5508eb |
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| Source note | uspto-grants-1986_08 |
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