Sodium Bicarbonate → 2-methoxy-1-[2-(5-{1-[5-(methylsulfanyl)pyridin-2-yl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)-1,3-thiazol-5-yl]ethanol

HRID 1882092Notes

Reaction equation

[OH:1][CH:2]([C:6]1[S:10][C:9]([C:11](=O)[CH2:12][CH2:13][C:14](=O)[CH:15]([C:23]2[CH:28]=[CH:27][C:26]([S:29][CH3:30])=[CH:25][N:24]=2)[CH2:16][CH:17]2[CH2:22][CH2:21][O:20][CH2:19][CH2:18]2)=[N:8][CH:7]=1)[CH2:3][O:4][CH3:5].C([O-])(=O)C.[NH4+:37].C(=O)([O-])O.[Na+]>C(O)(=O)C.C(OCC)(=O)C>[CH3:5][O:4][CH2:3][CH:2]([C:6]1[S:10][C:9]([C:11]2[NH:37][C:14]([CH:15]([C:23]3[CH:28]=[CH:27][C:26]([S:29][CH3:30])=[CH:25][N:24]=3)[CH2:16][CH:17]3[CH2:22][CH2:21][O:20][CH2:19][CH2:18]3)=[CH:13][CH:12]=2)=[N:8][CH:7]=1)[OH:1]

Participants

Conditions

Temperature: 110 °C

Procedure

To a solution of 1-[5-(1-hydroxy-2-methoxyethyl)-1,3-thiazol-2-yl]-5-[5-(methylsulfanyl)pyridin-2-yl]-6-(tetrahydro-2H-pyran-4-yl)hexane-1,4-dione (103 mg) in acetic acid (1.7 mL) was added ammonium acetate (265 mg), and the mixture was stirred at 110° C. for 1 hr. After cooling to room temperature, the mixture was neutralized with saturated aqueous sodium hydrogen carbonate solution. The reaction mixture was diluted with ethyl acetate and washed with water. The ethyl acetate layer was dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and the title compound (62.8 mg, yield 64%) was obtained as a pale-yellow amorphous solid from a fraction eluted with ethyl acetate-hexane (19:1, volume ratio).

Workup

temperatureAfter cooling to room temperature
washwashed with water
dry with materialThe ethyl acetate layer was dried (MgSO4)
concentrationconcentrated

Sources & evidence

ORD record: ord-7bc50f512d924eb582003d1b366be225
Source dataset: uspto-grants-2012_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08318746B2

Reaction notes

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