HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → methyl (13S,15R,16R,18S)-13-[(1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-10-hydroxy-5-methoxy-10-methoxycarbonyl-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraen-4-yl]-18-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.04,12.05,10.016,18]icosa-4(12),5,7,9-tetraene-13-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3',4'-Anhydrovinblastine | HCID 443324 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | methyl (13S,15R,16R,18S)-13-[(1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-10-hydroxy-5-methoxy-10-methoxycarbonyl-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraen-4-yl]-18-ethyl-17-oxa-1,11-diazapentacyclo[13.4.1.04,12.05,10.016,18]icosa-4(12),5,7,9-tetraene-13-carboxylate | HCID 442111 | — |
Reaction Steps
To a solution of 50 mg. of 3',4'-anhydro-vinblastine in 5 ml. of tetrahydrofuran 50 mg. of a 15% aqueous sodium hychlorite solution is added.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04199505 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-df3e84bb87ae4d89bf3ae58ed63a4f20 |
| Source note | uspto-grants-1980_04 |