HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 17-n-Propylamino-geldanamycin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Geldanamycin | HCID 5288382 | — |
| Solvent | Water | HCID 962 | — |
| Product | 17-n-Propylamino-geldanamycin | HCID 5472884 | 98% |
Reaction Steps
Into 50 ml. of chloroform, 280 mg. of Geldanamycin was dissolved and then, 1 ml. of n-propylamine was added. The mixture was stirred at room temperature for 1 hour and the mixture was charged into 50 ml. of cold water and then, pH was adjusted 3 with 6 N-HCl. The chloroform layer was separated and the water layer was extructed with 50 ml. of chloroform. Both chloroform layers were combined and dehydrated over anhydrous sodium sulfate for 2 hours. Chloroform was distilled off under a reduced pressure to remain a reddish violet solid product. The solid product was recrystallized from acetone-n-hexane to obtain 286 mg. (yield 98%) of 17-n-propylamino-Geldanamycin as reddish violet acicular crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04261989 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-2a91ab5206854ce1ab59095fb1054b7e |
| Source note | uspto-grants-1981_04 |