Hydrochloric Acid → HCID 178493316, compound
Reaction equation
[NH2:1][CH2:2][C:3]1[N:7]=[C:6]([C@H:8]2[NH:21][C:20](=[S:22])[CH2:19][CH2:18][CH2:17][CH2:16][O:15][C:14](=[O:23])[C:13]3[C:24]([CH3:40])=[C:25]([O:38][CH3:39])[CH:26]=[C:27]([O:28][Si](C)(C)C(C)(C)C(C)C)[C:12]=3[CH2:11][S:10][CH2:9]2)[O:5][N:4]=1.P([O-])([O-])([O-])=O.[Na+].[Na+].[Na+].[OH-].[Na+].Cl.[C:52](=[NH:57])(OCC)[CH3:53].Cl>>[OH:28][C:27]1[C:12]2[CH2:11][S:10][CH2:9][C@@H:8]([C:6]3[O:5][N:4]=[C:3]([CH2:2][NH:1][C:52](=[NH:57])[CH3:53])[N:7]=3)[NH:21][C:20](=[S:22])[CH2:19][CH2:18][CH2:17][CH2:16][O:15][C:14](=[O:23])[C:13]=2[C:24]([CH3:40])=[C:25]([O:38][CH3:39])[CH:26]=1Participants
Procedure
The pH of a suspension of 20 mg of the product of Example 130 in 3 ml of 0.05M pH7 sodium phosphate buffer was adjusted to 8.5 by the addition of 0.1N sodium hydroxide. Over 3 h, 74 mg of ethyl acetimidate hydrochloride were added in small portions, the pH of the reaction mixture being maintained at 8.5. The mixture was set to pH 7 by addition of 1N hydrochloric acid and then extracted with ethyl acetate. The aqueous phase was concentrated in vacuo and chromatographed on MCI-Gel CHP20P (Mitsubishi Chemical Industries, Ltd.) using at first 1% aqueous acetic acid and then mixtures of 1% aqueous acetic acid with acetonitrile (10:1 to 2:1, v/v). The product-containing fractions were lyophilized to yield 4 mg of (4R)-N-[5-(16-hydroxy-14-methoxy-13-methyl-12-oxo-6-thioxo-1,3,4,5,6,7,8,9,10,12-decahydro-11,2,5-benzoxathiaazacyclotetradecin-4-yl)-1,2,4-oxadiazol-3-ylmethyl]-acetimidamide hydroacetate.
Workup
- temperaturethe pH of the reaction mixture being maintained at 8.5
- extractionextracted with ethyl acetate
- concentrationThe aqueous phase was concentrated in vacuo
- customchromatographed on MCI-Gel CHP20P (Mitsubishi Chemical Industries, Ltd.)
Sources & evidence
- ORD record
- ord-eb6220133454480eb820cb4d5d3608d6
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05594135
Reaction notes
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