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Chemical Structure| 870812-93-4 Chemical Structure| 870812-93-4

Structure of 870812-93-4

Chemical Structure| 870812-93-4

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Product Details of [ 870812-93-4 ]

CAS No. :870812-93-4
Formula : C22H26N2O4S
M.W : 414.52
SMILES Code : O=C(N1CCOCC1)C[C@@H](NC(OCC2=CC=CC=C2)=O)CSC3=CC=CC=C3
MDL No. :MFCD16659953

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Application In Synthesis of [ 870812-93-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 870812-93-4 ]

[ 870812-93-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 870812-93-4 ]
  • [ 870812-94-5 ]
YieldReaction ConditionsOperation in experiment
~ 100% A suspension of (R)-benzyl 4-morpholino-4-oxo-1-(phenylthio)butan-2-ylcarbamate (INTERMEDIATE 71, 25 g, 60 mmol) in 40% HBr in acetic acid (500 ml) was stirred at room temperature for 50 hrs. The reaction mixture became homogeneous during this time. The reaction mixture was concentrated to dryness, diluted with water (400 ml) and 5% aq. HCl (200 ml) and washed with diethyl ether (3*100 ml). The aqueous phase was brought to pH ~8-9 with solid Na2CO3 and extracted vigorously with CH2Cl2 (5*). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to give the title product (16.9 g, yield: almost quantitative), which was used in the preparation of Intermediate 73 without further purification. 1H-NMR (300 MHz, DMSO-d6) delta 2.42 (dd, 1H), 2.57 (dd, 1H), 2.77 (m 3H), 2.97-3.02 (m, 1H), 3.06-3.14 (m, 1H), 3.37 (m, 2H), 3.59 (m, 6H), 7.18 (t, 1H), 7.27 (d, 2H), 7.37 (d, 2H). LCMS: (ESI) m/z 281 (M+H)+.
98% With hydrogen bromide; acetic acid; at 20℃; for 24h; EXAMPLE 21E (1R)-3-(4-morpholinyl)-3-oxo-1-((phenylsulfanyl)methyl)propylamine A solution of EXAMPLE 21D (18.0 g, ~39 mmol) in 30% HBr in acetic acid (250 mL) was stirred for 24 hours at room temperature, concentrated to half its volume, poured into 1M HCl (300 mL), washed with diethyl ether (3*200 mL), and extracted with 1M HCl (150 mL). The combined aqueous layers were cooled to 0 C., adjusted to pH ~12 with solid KOH, and extracted with dichloromethane (5*100 mL). The combined extracts were washed with brine, dried (Na2SO4), filtered, and concentrated to provide the desired product (10.8 g, 98%).
93% A solution of intermediate g 4g, 9.7 mmol) in 30% HBr in acetic acid (40 ml) was stirred for 24 hours at room temperature, concentrated to half its volume, poured into IM HCl (40 ml) . The combined aqueous layers were washed with ether (3X50 mL) and cooled to 0 0C, adjusted to 12 with solid KOH, and extracted with CH2Cl2. The combined extracts were washed with brine, dried (Na2SO4), filtered, and concentrated to provide the desired product h (2.5g, yield:93%). MS (ESI) m/e (M+H^):281; 1H- NMR (CDCl3, 400 MHz): delta 7.31 (d, J= 8.0 Hz, 2H), 7.21 (t, J= 7.6 Hz, 2H), 7.12 (t, J = 7.6 Hz, IH), 3.58-3.50 (m, 6H), 3.38-3.30 (m, 3H), 3.05 (m, IH), 2.87 (m, IH), 2.50 (m, IH), 2.28 (m, IH).
 

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