반응식
[OH:1][C:2]1[N:6]([CH3:7])[N:5]=[C:4]([C:8]([OH:10])=O)[CH:3]=1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CN(C=O)C.[CH2:40]([O:42][C:43](=[O:63])[C@H:44]([OH:62])[CH2:45][C@H:46]([NH2:61])[CH2:47][C:48]1[CH:53]=[CH:52][C:51]([C:54]2[CH:59]=[CH:58][CH:57]=[C:56]([Cl:60])[CH:55]=2)=[CH:50][CH:49]=1)[CH3:41].CCN(C(C)C)C(C)C>>[CH2:40]([O:42][C:43](=[O:63])[C@H:44]([OH:62])[CH2:45][C@H:46]([NH:61][C:8]([C:4]1[CH:3]=[C:2]([OH:1])[N:6]([CH3:7])[N:5]=1)=[O:10])[CH2:47][C:48]1[CH:53]=[CH:52][C:51]([C:54]2[CH:59]=[CH:58][CH:57]=[C:56]([Cl:60])[CH:55]=2)=[CH:50][CH:49]=1)[CH3:41]참가 물질
6
반응물 5
생성물 1
실험 절차
5-Hydroxy-1-methyl-1h-pyrazole-3-carboxylic acid (122 mg, 862 μmol) and HATU (361 mg, 949 μmol) were combined in DMF (1.0 mL, 13 mmol) and stirred for 10 minutes. (2R,4R)-4-amino-5-(3′-chlorobiphenyl-4-yl)-2-hydroxypentanoic acid ethyl ester (30.0 mg, 86 μmol) and DIPEA (165 μL, 949 μmol) were added, and the resulting mixture was stirred at room temperature overnight. The mixture was then concentrated under reduced pressure and the residue was dissolved in 50% AcOH-water (1.5 mL), filtered, purified by reverse phase preparative HPLC, and lyophilized to yield the title compound (11.1 mg). MS m/z [M+H]+ calc'd for C24H26ClN3O5, 472.16. found 472.2.
후처리
- stirringthe resulting mixture was stirred at room temperature overnight
- concentrationThe mixture was then concentrated under reduced pressure
- dissolutionthe residue was dissolved in 50% AcOH-water (1.5 mL)
- filtrationfiltered
- custompurified by reverse phase preparative HPLC
출처 및 근거
- ORD 기록
- ord-a1e22c1b7ca94f548df0a5cbf19ac39c
- 출처 데이터셋
- uspto-grants-2015_08
- 특허 번호
- US09108934B2
연결된 노트
불러오는 중…