Hydrochloric Acid → rac-(2R,3R,4R,5S)-4-(4-chloro-2,6-difluoro-phenyl)-3-(3-chloro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carboxylic acid ((S)-3,4-dihydroxy-butyl)-amide

HRID 1806957노트

반응식

HRID 1806957 반응식
FC(F)(F)C(O)=O.[Cl:8][C:9]1[CH:14]=[C:13]([F:15])[C:12]([C:16]2([C:36]#[N:37])[CH:20]([CH2:21][C:22]([CH3:25])([CH3:24])[CH3:23])[NH:19][CH:18]([C:26]([OH:28])=O)[CH:17]2[C:29]2[CH:34]=[CH:33][CH:32]=[C:31]([Cl:35])[CH:30]=2)=[C:11]([F:38])[CH:10]=1.CC1(C)[O:44][C@@H:43]([CH2:45][CH2:46][NH2:47])[CH2:42][O:41]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.Cl>C(Cl)Cl.O1CCCC1>[OH:44][C@H:43]([CH2:42][OH:41])[CH2:45][CH2:46][NH:47][C:26]([CH:18]1[CH:17]([C:29]2[CH:34]=[CH:33][CH:32]=[C:31]([Cl:35])[CH:30]=2)[C:16]([C:12]2[C:11]([F:38])=[CH:10][C:9]([Cl:8])=[CH:14][C:13]=2[F:15])([C:36]#[N:37])[CH:20]([CH2:21][C:22]([CH3:23])([CH3:24])[CH3:25])[NH:19]1)=[O:28]

참가 물질

8

실험 절차

In a manner similar to the method described in Examples 42c, 42d, rac-(2R,3R,4R,5S)-4-(4-chloro-2,6-difluoro-phenyl)-3-(3-chloro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carboxylic acid trifluoroacetic acid prepared in Example 108c (0.4 g, 0.67 mmol) was reacted with 2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethylamine (0.29 g, 2 mmol), HATU (0.46 g, 1.2 mmol) and iPr2NEt (0.58 mL, 3.3 mmol) in CH2Cl2 at room temperature for 20 h, then reacted with aqueous HCl solution in tetrahydrofuran at room temperature for 2 h to give rac-(2R,3R,4R,5S)-4-(4-chloro-2,6-difluoro-phenyl)-3-(3-chloro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carboxylic acid ((S)-3,4-dihydroxy-butyl)-amide as a white solid (0.3 g, 77%).

출처 및 근거

ORD 기록
ord-f30098356a184f74b81d74833938dcea
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08354444B2

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