Ammonia → (S)-4-Amino-N-(1-cyano-2-(4-(1-oxoisoindolin-5-yl)phenyl)ethyl)tetrahydro-2H-pyran-4-carboxamide

HRID 216940Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 216940
[C:1]([C@@H:3]([NH:21][C:22]([C:24]1([NH:30]C(=O)OC(C)(C)C)[CH2:29][CH2:28][O:27][CH2:26][CH2:25]1)=[O:23])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[C:16](=[O:20])[NH:15][CH2:14]3)=[CH:7][CH:6]=1)#[N:2].N>C(O)=O.O>[NH2:30][C:24]1([C:22]([NH:21][C@H:3]([C:1]#[N:2])[CH2:4][C:5]2[CH:6]=[CH:7][C:8]([C:11]3[CH:12]=[C:13]4[C:17](=[CH:18][CH:19]=3)[C:16](=[O:20])[NH:15][CH2:14]4)=[CH:9][CH:10]=2)=[O:23])[CH2:29][CH2:28][O:27][CH2:26][CH2:25]1

Komponenten

5

Versuchsvorschrift

(S)-tert-Butyl 4-(1-cyano-2-(4-(1-oxoisoindolin-5-yl)phenyl)ethylcarbamoyl)tetrahydro-2H-pyran-4-ylcarbamate (Example 15, step (ii), 160 mg) was stirred in formic acid (0.5 mL) at 50° C. for 20 min. The reaction mixture was cooled to room temperature and the mixture diluted with water (20 mL). The solution was basified with 0.880 ammonia and extracted into ethyl acetate (100 mL). The extract was dried over magnesium sulfate and concentrated. The crude product was purified by chromatography on silica using methanol/ethyl acetate (1/9) to afford the titled compound as a solid (70 mg).

Aufarbeitung

  1. extractionextracted into ethyl acetate (100 mL)
  2. dry with materialThe extract was dried over magnesium sulfate
  3. concentrationconcentrated
  4. customThe crude product was purified by chromatography on silica

Quellen und Nachweise

ORD-Eintrag
ord-cf8de84d06b04181b7b8564b4982ecba
Quelldatensatz
uspto-grants-2012_06
Patentnummer
US08193239B2

Notizen zur Reaktion

Wird geladen…