Trifluoroacetic acid → HCID 131714601, compound
Reaction equation
[NH2:1][C@H:2]([C:5]([NH:7][C@H:8]([C:10]([O:12][CH3:13])=[O:11])[CH3:9])=[O:6])[CH2:3][OH:4].C(O)(C(F)(F)F)=O.[NH:21]([C:30]([O:32][C:33]([CH3:36])([CH3:35])[CH3:34])=[O:31])[C@H:22]([C:27](O)=[O:28])[CH2:23][CH:24]([CH3:26])[CH3:25].F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1>CN(C=O)C.C(Cl)(Cl)Cl.CCOCC.CCCCCC.O>[NH:21]([C:30]([O:32][C:33]([CH3:35])([CH3:34])[CH3:36])=[O:31])[C@H:22]([C:27]([NH:1][C@H:2]([C:5]([NH:7][C@H:8]([C:10]([O:12][CH3:13])=[O:11])[CH3:9])=[O:6])[CH2:3][OH:4])=[O:28])[CH2:23][CH:24]([CH3:26])[CH3:25]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 5
Procedure
40 g of H-Ser-Ala-OMe, TFA and 32.9 g of Boc-Leu-OH, H2O are dissolved in 400 ml of DMF. The product is cooled with an ice bath with magnetic stirring and 14.4 ml of NEM then 65.8 g of BOP and enough NEM to maintain the pH at 6.5-7 are added. The product is stirred for 2 hrs. at ambient temperature. After monitoring by TLC, the product is evaporated to dryness (13.33 Pa35° C.) and the oil obtained is dissolved in 1500 ml of chloroform, washed twice with a saturated NaCl solution, three times with 5% potassium sulfate/bisulfate, 3 times with saturated sodium bicarbonate, dried over Na2SO4, evaporated to dryness (30°--water-jet pump). The oil obtained is solidified in ether : Fraction A=29 g. A second jet B is obtained by addition of hexane, identical in TLC : B=13.7 g.
Workup
- temperatureThe product is cooled with an ice bath
- additionare added
- stirringThe product is stirred for 2 hrs
- customat ambient temperature
- customthe product is evaporated to dryness (13.33 Pa35° C.)
- customthe oil obtained
- washwashed twice with a saturated NaCl solution, three times with 5% potassium sulfate/bisulfate, 3 times with saturated sodium bicarbonate
- dry with materialdried over Na2SO4
- customevaporated to dryness (30°--water-jet pump)
- customThe oil obtained
Sources & evidence
- ORD record
- ord-a40a799195114930a40fd5c95c5d2787
- Source dataset
- uspto-grants-1987_11
- Patent number
- US04707541
Reaction notes
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