HuagongsheHuagongshe Chemistry Print Report · For research reference only
((p-(Benzyloxy)phenoxy)methyl)oxirane → HCID 20237810, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ((p-(Benzyloxy)phenoxy)methyl)oxirane | HCID 119882 | — |
| Reactant | HCID 12818868 | HCID 12818868 | — |
| Reactant | HCID 20237871 | HCID 20237871 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20237810 | HCID 20237810 | — |
Reaction Steps
The 1-(4-benzyloxyphenoxy)-3-[2-(indazol-4-ylamino)-ethylamino]-propan-2-ol used as starting material can be obtained in the following manner: 5.1 g. 4-benzyloxyphenyl glycidyl ether and 7.0 g. 4-(2-aminoethylamino)-indazole are dissolved in 10 ml. dimethylformamide and left to stand for 2 days at ambient temperature. The reaction mixture is then digested by the addition of 20 ml. methanol, filtered off with suction and then washed with methanol. There are obtained 5.0 g. (58% of theory) of the desired product in the form of colorless crystals; m.p. 151°-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04608383 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-5854121105854a75ac7c5139884db7c4 |
| Source note | uspto-grants-1986_08 |