HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tacrolimus-13C,D2 → HCID 57266865, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tacrolimus-13C,D2 | HCID 5372 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57266865 | HCID 57266865 | — |
Reaction Steps
To a stirred solution of 17-allyl-1,14-dihydroxy-12-[2'-(4"-hydroxy-3"-methoxycyclohexyl)-1'-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone (108 mg, 0.135 mmol) in 4 ml MeOH cooled to -5° C. (ice/acetone bath) was added in several portions NaBH3CN (160 mg). After addition was complete reaction was allowed to warm to RT. After stirring at RT for 2 hours the reaction mixture was diluted with 10 ml CH2Cl2 and purified by prep TLC (5% MeOH/CH2Cl2) to give the title compound (with NMR and mass spectra consistent with the structure).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05064835 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-af9e5395f0564dc0b1cde7782334bf18 |
| Source note | uspto-grants-1991_11 |