Trifluoroacetic acid → HCID 86698935, Verbindung
Reaktionsgleichung
[O:1]=[C:2]([CH2:49][CH2:50][CH2:51][C:52](=[O:72])[NH:53][C:54]1[CH:55]=[N:56][C:57]([C:60]2[N:61]=[N:62][C:63]([C:66]3[CH:71]=[CH:70][CH:69]=[CH:68][N:67]=3)=[N:64][N:65]=2)=[CH:58][CH:59]=1)[NH:3][CH2:4][CH2:5][O:6][CH2:7][CH2:8][O:9][CH2:10][CH2:11][O:12][CH2:13][CH2:14][O:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][O:21][CH2:22][CH2:23][O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29][O:30][CH2:31][CH2:32][O:33][CH2:34][CH2:35][O:36][CH2:37][CH2:38][O:39][CH2:40][CH2:41][C:42]([O:44]C(C)(C)C)=[O:43].C(O)(C(F)(F)F)=O>C(Cl)Cl>[O:1]=[C:2]([CH2:49][CH2:50][CH2:51][C:52](=[O:72])[NH:53][C:54]1[CH:55]=[N:56][C:57]([C:60]2[N:61]=[N:62][C:63]([C:66]3[CH:71]=[CH:70][CH:69]=[CH:68][N:67]=3)=[N:64][N:65]=2)=[CH:58][CH:59]=1)[NH:3][CH2:4][CH2:5][O:6][CH2:7][CH2:8][O:9][CH2:10][CH2:11][O:12][CH2:13][CH2:14][O:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][O:21][CH2:22][CH2:23][O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29][O:30][CH2:31][CH2:32][O:33][CH2:34][CH2:35][O:36][CH2:37][CH2:38][O:39][CH2:40][CH2:41][C:42]([OH:44])=[O:43]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of 3 (160 mg, 0.157 mmol) in anhydrous DCM (2 mL) under nitrogen atmosphere was added TFA (2 mL). The reaction mixture was stirred for 2 hours at room temperature and evaporated to dryness. The residue was redissolved in dry DCM (2 ml) and again treated with TFA (2 mL) for 2 hours. This process was repeated once more. Finally, the reaction mixture was evaporated to dryness and co-evaporated twice with DCM furnishing the deprotected product 4 in quantitative yield.
Aufarbeitung
- customevaporated to dryness
- dissolutionThe residue was redissolved in dry DCM (2 ml)
- additionagain treated with TFA (2 mL) for 2 hours
- customFinally, the reaction mixture was evaporated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-cb9234b744654160b2207c209bf8dbb0
- Quelldatensatz
- uspto-grants-2016_08
- Patentnummer
- US09427482B2
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