Nitrogen → HCID 57079368, compound
Reaction equation
[CH3:1][C:2]1[C@@H:3]2[C@@H:19]([C@:20]3([CH3:28])[C:25]([CH:26]=1)=[CH:24][C:23](=[O:27])[CH2:22][CH2:21]3)[CH2:18][CH2:17][C@@:16]1([CH3:29])[C@H:4]2[CH2:5][CH2:6][C@@H:7]1[C@H:8]([CH3:15])[CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12].C1CCCCC=1.N#N>[Pd].C(O)C>[CH3:1][C@H:2]1[CH2:26][C:25]2[C@:20]([CH3:28])([CH2:21][CH2:22][C:23](=[O:27])[CH:24]=2)[C@@H:19]2[C@@H:3]1[C@H:4]1[C@:16]([CH3:29])([CH2:17][CH2:18]2)[C@@H:7]([C@H:8]([CH3:15])[CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12])[CH2:6][CH2:5]1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of methyl 7-methyl-3-oxochola-4,6-dien-24-oate (9) (0.62 g, 1.56 mmoles), 5% palladium on carbon (72 mg), 1, 8-diazobicyclo[5.4.0]undec-7-ene (15 ml), cyclohexene (4.9 ml) and ethanol (3.6 ml) was heated under reflux in an N2 for 6 hrs. The cooled mixture was filtered, and the catalyst washed with ethanol (4 times). The combined filtrate and washes were evaporated in vacuo . The residue was dissolved in EtOAc (30 ml), washed with 0.5M HCl, H2O, saturated brine and dried (MgSO4). Evaporation in vacuo gave 0.62 g of pure 10 as a pale yellow syrup. NMR (CDCl3): δ 0.71 (s, 3H, 18-Me); 0.94 (d, 3H, 20-Me); 1.05 (d, 3H, 7-Me); 1.15 (s, 3H, 19-Me); 3.66 (s, 3H, CO2Me); 5.70 (s, 1H, 4-H).
Workup
- temperaturewas heated
- filtrationThe cooled mixture was filtered
- washthe catalyst washed with ethanol (4 times)
- customThe combined filtrate and washes were evaporated in vacuo
- dissolutionThe residue was dissolved in EtOAc (30 ml)
- washwashed with 0.5M HCl, H2O, saturated brine
- dry with materialdried (MgSO4)
- customEvaporation in vacuo
Sources & evidence
- ORD record
- ord-c1c20049d07f4371986226b52bf3cefd
- Source dataset
- uspto-grants-1998_12
- Patent number
- US05843953
Reaction notes
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