Hydrochloric Acid → 2-{3-[(2,2-Difluoro-2-phenylethyl)amino]-6-chloro-2-fluorophenyl}acetic Acid
반응식
Cl([O-])=[O:2].[Na+].[F:5][C:6]([F:26])([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH2:7][NH:8][C:9]1[C:10]([F:19])=[C:11]([CH2:16][CH:17]=[O:18])[C:12]([Cl:15])=[CH:13][CH:14]=1.Cl>O.CS(C)=O>[F:26][C:6]([F:5])([C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)[CH2:7][NH:8][C:9]1[C:10]([F:19])=[C:11]([CH2:16][C:17]([OH:2])=[O:18])[C:12]([Cl:15])=[CH:13][CH:14]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
A solution of sodium chlorite (692 mg, 6.11 mmol) in H2O (6.1 mL) was added over a period of 30 minutes to a stirred mixture of 2{-3-[(2,2-difluoro-2-phenylethyl)amino]-6-chloro-2-fluorophenyl}ethanal (1.43 g, 4.37 mmol), as prepared in the preceding step, in DMSO (4.5 mL) and of NaH2PO4 (141 mg, 1.18 mmol) in H2O (1.7 mL). After the addition, the mixture was stirred at ambient temperature overnight, acidified with 10 M HCl to pH 1, and extracted with DCM (3 times). The extracts were combined, washed with H2O and brine, dried over Na2SO4, and concentrated in vacuo. The resulting residue was flash chromatographed on silica gel eluting with MeOH/DCM (0, 2, and 4%) to give the title compound (0.77 g, 51% yield) as a pale brown solid. 1H-NMR (400 MHz, CD3OD) δ 7.53-7.51 (m, 2H), 7.44-7.41 (m, 3H), 6.93 (dd, J=8.9, 1.8 Hz, 1H), 6.62 (t, J=9.1 Hz, 1H), 3.80 (t, J=13.7 Hz, 2H), 3.74 (d, J=2.2 Hz, 2H). Mass spectrum (LCMS, ESI) calc'd for C16H14ClF3NO2 (M+H): 344.1. Found: 344.4.
후처리
- additionAfter the addition
- extractionextracted with DCM (3 times)
- washwashed with H2O and brine
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customchromatographed on silica gel eluting with MeOH/DCM (0, 2, and 4%)
출처 및 근거
- ORD 기록
- ord-bae833267f9d4a0a879bed8a0af6573d
- 출처 데이터셋
- uspto-grants-2005_05
- 특허 번호
- US06900231B2
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