Cyclohexanemethylamine → (1r,2s)-1-{[(2s,4r)-1-[(1S)-1-(cyclohexylmethyl-carbamoyl)-2,2-dimethyl-propylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}-2-vinyl-cyclopropanecarboxylic acid

HRID 1822444ノート

反応式

HRID 1822444 の反応式
C(OC(N[C@H](C(O)=O)C(C)(C)C)=O)(C)(C)C.C(OC(NC(C(C)(C)C)C(O)=O)=O)(C)(C)C.[CH:33]1([CH2:39][NH2:40])[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1.C(OC(=O)NC(C(=O)NC1C2C(=CC=CC=2)CC1O)C(C)(C)C)(C)(C)C.ClNC(=O)[O-].C([O:74][C:75]([C:77]1([NH:82][C:83]([CH:85]2[CH2:89][CH:88]([O:90][C:91]3[C:100]4[C:95](=[CH:96][C:97]([O:101][CH3:102])=[CH:98][CH:99]=4)[N:94]=[C:93]([C:103]4[CH:108]=[CH:107][CH:106]=[CH:105][CH:104]=4)[CH:92]=3)[CH2:87][N:86]2[C:109](=[O:129])[NH:110][CH:111]([C:116](=[O:128])NC2C3C(=CC=CC=3)CC2O)[C:112]([CH3:115])([CH3:114])[CH3:113])=[O:84])[CH2:79][CH:78]1[CH:80]=[CH2:81])=[O:76])C>>[CH:33]1([CH2:39][NH:40][C:116]([C@@H:111]([NH:110][C:109]([N:86]2[CH2:87][C@H:88]([O:90][C:91]3[C:100]4[C:95](=[CH:96][C:97]([O:101][CH3:102])=[CH:98][CH:99]=4)[N:94]=[C:93]([C:103]4[CH:108]=[CH:107][CH:106]=[CH:105][CH:104]=4)[CH:92]=3)[CH2:89][C@H:85]2[C:83]([NH:82][C@:77]2([C:75]([OH:76])=[O:74])[CH2:79][C@H:78]2[CH:80]=[CH2:81])=[O:84])=[O:129])[C:112]([CH3:115])([CH3:114])[CH3:113])=[O:128])[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1

参加物

7

反応物 6

HCID 76688CyclohexanemethylamineHCID 2734668(S)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acidHCID 50468592-{[(Tert-butoxy)carbonyl]amino}-3,3-dimethylbutanoic acidHCID 22035886ChlorocarbamateHCID 68488177[1-(2-Hydroxy-indan-1-ylcarbamoyl)-2,2-dimethyl-propyl]-carbamic acid tert.butyl esterHCID 684916281-{[1-[1-(2-Hydroxy-indan-1-ylcarbamoyl)-2,2-dimethyl-propylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}-2-vinyl-cyclopropanecarboxylic acid ethyl ester

生成物 1

HCID 68494906(1r,2s)-1-{[(2s,4r)-1-[(1S)-1-(cyclohexylmethyl-carbamoyl)-2,2-dimethyl-propylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}-2-vinyl-cyclopropanecarboxylic acid

実験手順

N-(tert-butoxycarbonyl)-L-tert-butylglycine was attached to the resin as described for the preparation of compound 16 followed by reaction with cyclohexanemethylamine as described for the preparation of 17 and removal of the Boc group as described for 18. The afforded compound was then reacted with the chlorocarbamate achieved from 12 as described for the preparation of 13 which gave the title compound. Purity by HPLC>95%. M+H+726.3.

出典と根拠

ORDレコード
ord-0a0ba1b1b8a84f909093d6ff1ce3b5a9
出典データセット
uspto-grants-2009_10
特許番号
US07608590B2

反応ノート

読み込み中…