1,2-Dichloroethane → HCID 136381122, Verbindung

HRID 53579Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 53579
C(OC[C:6]1[CH2:13][S:12][CH:11]2[N:8]([C:9](=[O:30])[CH:10]2[NH:14][C:15](=[O:29])[CH2:16][C:17]2[N:18]=[C:19]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[OH:28])[S:20][CH:21]=2)[C:7]=1[C:31]([OH:33])=[O:32])(=O)C.[SiH](CC)(CC)CC.FC(F)(F)C(O)=O.C(Cl)C[Cl:50]>>[Cl:50][C:6]1[CH2:13][S:12][CH:11]2[N:8]([C:9](=[O:30])[CH:10]2[NH:14][C:15](=[O:29])[CH2:16][C:17]2[N:18]=[C:19]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[OH:28])[S:20][CH:21]=2)[C:7]=1[C:31]([OH:33])=[O:32]

Komponenten

5

Versuchsvorschrift

The procedure used for the preparation of 9a was repeated with 8b (390 mg, crude from previous reaction), Et3SiH (0.80 mL, 5.0 mmol), and trifluoroacetic acid (1.50 mL, 19.5 mmol ) in dry ClCH2CH2Cl (8 mL ) at 0° C. under nitrogen to give 9b (50.0 mg, 35% for two steps) as a white solid after chromatographic separation on RP C-18 (gradient CH3CN/H2O: 25-30%, containing 1% HOAc). mp 155° C. (dec); IR (KBr) 3600-2800 (br), 3280, 1780, 1661 cm-1 ; 1H NMR (DMSO-d6) δ3.63 (1H, d, J=18.0 Hz), 3.74 (2H, s, CH2), 3.93 (1H, d, J=18.0 Hz), 5.15 (1H, d, J=4.7 Hz), 5.70 (1H, dd, J=8.0 and 4.7 Hz), 6.88 (1H, t, J=7.7 Hz), 6.96 (1H, d, J=7.7 Hz), 7.25 (1H, t, J=7.7 Hz), 7.40 (1H, s), 7.94 (1H, d, J=7.7 Hz), 9.16 (1H, d, J=8.0 Hz, NH), 11.30 (1H, s, OH), 13.80 (1H, br s, CO2H); FDMS m/z 451 (M+, 35Cl), 452 (M+ +1, 35Cl), 453 (M+, 37Cl), 454 (M+ +1, 37Cl); Anal. Calcd for C18H14ClN3O5S2 : C, 47.84; H, 3.12; N, 9.30. Found: C, 48.12; H, 3.16; N, 9.36

Quellen und Nachweise

ORD-Eintrag
ord-0eeeb878638140c5af1a7eb280dbdbff
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05620968

Notizen zur Reaktion

Wird geladen…