Dimethylformamide → O-{[(3-sulfophenyl)amino]carbonyl}-L-serine
반응식
[NH:1](C(OC(C)(C)C)=O)[C@H:2]([C:5]([O:7]C(C)(C)C)=[O:6])[CH2:3][OH:4].N[C:20]1[CH:21]=[C:22]([S:26]([OH:29])(=[O:28])=[O:27])C=CC=1.CN(C=[O:34])C.C([N:38]([CH:41]([CH3:43])[CH3:42])[CH2:39]C)(C)C>C(Cl)Cl.C(O)(C(F)(F)F)=O>[S:26]([C:22]1[CH:43]=[C:41]([NH:38][C:39]([O:4][CH2:3][C@@H:2]([C:5]([OH:7])=[O:6])[NH2:1])=[O:34])[CH:42]=[CH:20][CH:21]=1)([OH:29])(=[O:28])=[O:27]참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
Boc-Ser-OtBu (200 mg, 0.77 mmol) was dissolved in 3 ml of methylene chloride and cooled to 0° C. N,N′-Carbonyldiimidazole (124 mg, 0.77 mmol) was added to the solution and stirred at room temperature for 2 hours. After the solvent was removed by distillation, 3-aminobenzenesulfonic acid (132.6 mg, 0.77 mmol), 2 ml of DMF and 0.4 ml of diisopropylethylamine were added and stirred at 70° C. overnight. The solvent was removed by distillation and the mixture was purified according to the purification step A to give the intermediate. The resulting intermediate was dissolved in 1 ml of TFA and stirred at room temperature for 2 hours. The solvent was removed by distillation, and the mixture was purified according to the purification step A to give the title compound.
후처리
- additionwere added
- stirringstirred at 70° C. overnight
- customThe solvent was removed by distillation
- customthe mixture was purified
- customaccording to the purification step A
- customto give the intermediate
- stirringstirred at room temperature for 2 hours
- customThe solvent was removed by distillation
- customthe mixture was purified
- customaccording to the purification step A
출처 및 근거
- ORD 기록
- ord-a494a03bbd9548e6be718b833d9176ee
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08877739B2
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