Diisopropylethylamine → 2-{4-(2-({(2-(4-Chlorophenyl)-1,3-thiazol-4-yl)methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl)phenoxy}ethyl N-(tert-butoxycarbonyl)-L-alanyl-L-alaninate

HRID 1968299ノート

反応式

HRID 1968299 の反応式
[C:1]([O:5][C:6]([NH:8][C@H:9]([C:11]([OH:13])=O)[CH3:10])=[O:7])([CH3:4])([CH3:3])[CH3:2].Cl.CN(C)CCCN=C=NCC.O.ON1C2C=CC=CC=2N=N1.C(N(CC)C(C)C)(C)C.FC(F)(F)C(O)=O.[NH2:53][C@H:54]([C:56]([O:58][CH2:59][CH2:60][O:61][C:62]1[CH:67]=[CH:66][C:65]([C:68]2[C:73]([C:74]#[N:75])=[C:72]([N:76]3[CH2:80][CH2:79][CH2:78][CH2:77]3)[N:71]=[C:70]([S:81][CH2:82][C:83]3[N:84]=[C:85]([C:88]4[CH:93]=[CH:92][C:91]([Cl:94])=[CH:90][CH:89]=4)[S:86][CH:87]=3)[C:69]=2[C:95]#[N:96])=[CH:64][CH:63]=1)=[O:57])[CH3:55]>CN(C=O)C.O>[C:1]([O:5][C:6]([NH:8][C@H:9]([C:11]([NH:53][C@H:54]([C:56]([O:58][CH2:59][CH2:60][O:61][C:62]1[CH:67]=[CH:66][C:65]([C:68]2[C:73]([C:74]#[N:75])=[C:72]([N:76]3[CH2:77][CH2:78][CH2:79][CH2:80]3)[N:71]=[C:70]([S:81][CH2:82][C:83]3[N:84]=[C:85]([C:88]4[CH:89]=[CH:90][C:91]([Cl:94])=[CH:92][CH:93]=4)[S:86][CH:87]=3)[C:69]=2[C:95]#[N:96])=[CH:64][CH:63]=1)=[O:57])[CH3:55])=[O:13])[CH3:10])=[O:7])([CH3:2])([CH3:3])[CH3:4]

参加物

8

反応物 5

HCID 81531DiisopropylethylamineHCID 85082Tert-butoxycarbonylalanineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 687647022-{4-(2-({(2-(4-chlorophenyl)-1,3-thiazol-4-yl)methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl)phenoxy}ethyl L-alaninate trifluoroacetate

生成物 1

HCID 594356502-{4-(2-({(2-(4-Chlorophenyl)-1,3-thiazol-4-yl)methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl)phenoxy}ethyl N-(tert-butoxycarbonyl)-L-alanyl-L-alaninate

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

26.756 g (141.406 mmol) of N-(tert-butoxycarbonyl)-L-alanine together with 29.572 g (154.261 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 29.529 g (192.827 mmol) of 1-hydroxy-1H-benzotriazole hydrate and 55.979 ml (321.378 mmol) of N,N-diisopropylethylamine were dissolved in 10 l DMF. 97.60 g (128.551 mmol) of trifluoroacetic acid-2-{4-(2-({(2-(4-chlorophenyl)-1,3-thiazol-4-yl)methyl}sulfanyl)-3,5-dicyano-6-(pyrrolidin-1-yl)pyridin-4-yl)phenoxy}ethyl L-alaninate (1:1) were then added, and the mixture was stirred at room temperature for 3 h. The reaction mixture was stirred into water and extracted with dichloromethane. The organic phase was washed with water, dried over sodium sulfate, filtered and concentrated. The residue was triturated with diethyl ether, and the solid was filtered off with suction and air-dried. This gave 95 g (91% of theory) of the desired target compound.

後処理

  1. extractionextracted with dichloromethane
  2. washThe organic phase was washed with water
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was triturated with diethyl ether
  7. filtrationthe solid was filtered off with suction
  8. customair-dried

出典と根拠

ORDレコード
ord-5585a0177b574219983de67a47514403
出典データセット
uspto-grants-2013_04
特許番号
US08420825B2

反応ノート

読み込み中…