반응식
[CH2:1]([O:8][C:9]([NH:11][C:12]1[C:13](=[O:22])[N:14]([CH2:18][C:19]([OH:21])=O)[CH:15]=[CH:16][CH:17]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.C1C=CC2N(O)N=NC=2C=1.CCN(C(C)C)C(C)C.[CH2:64]([CH:66]([CH2:69][CH3:70])[CH2:67][NH2:68])[CH3:65]>CN(C=O)C>[CH2:1]([O:8][C:9](=[O:10])[NH:11][C:12]1[C:13](=[O:22])[N:14]([CH2:18][C:19]([NH:68][CH2:67][CH:66]([CH2:69][CH3:70])[CH2:64][CH3:65])=[O:21])[CH:15]=[CH:16][CH:17]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
7
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
A mixture of 3.70 g of 2-(3-(benzyloxycarbonylamino)-2-oxopyridin-1(2H)-yl)acetic acid (˜11.2 mmol), 3.58 g of TBTU (11.2 mmol), 1.51 g of HOBt (11.2 mmol) is dissolved in 60 mL of DMF. By addition of 5.70 mL of DIPEA (33.5 mmol, 3 eq) a pH value is adjusted to ˜10. 1.50 mL of 2-ethyl-butylamine (11.2 mmol) is added and the mixture is stirred at RT overnight. The solvent is removed in vacuo and the obtained residue is taken up in 300 mL of DCM and subsequently washed with 10% citric acid (3×75 mL), saturated NaHCO3 solution (3×75 mL) and brine (75 mL). The organic phase is dried over Na2SO4, filtered and concentrated in dryness. Pale brown solid is obtained and it is suitable for further processing without further purification.
후처리
- customThe solvent is removed in vacuo
- washsubsequently washed with 10% citric acid (3×75 mL), saturated NaHCO3 solution (3×75 mL) and brine (75 mL)
- dry with materialThe organic phase is dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in dryness
- customPale brown solid is obtained
- customit is suitable for further processing without further purification
출처 및 근거
- ORD 기록
- ord-95502cae39944280b66e93911e468eb4
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09434763B2
연결된 노트
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