Methanol → HCID 3027864, compound

HRID 2036267Notes

Reaction equation

HRID 2036267 reaction equation
[CH3:1][C:2]([O:5][C:6]([NH:8][C:9]([NH:18]C(OC(C)(C)C)=O)=NS(C(F)(F)F)(=O)=O)=[O:7])([CH3:4])[CH3:3].CCN(C(C)C)C(C)C.C[OH:36]>>[C:6]([NH:8][C:9]([NH2:18])=[O:36])([O:5][C:2]([CH3:4])([CH3:3])[CH3:1])=[O:7]

Participants

4

Procedure

To a solution of amine 90 (300 mg, 0.62 mmol) and Goodman's reagent (392 mg, 1.00 mmol) in MeOH (60 mL) was added DIPEA (0.45 mL, 2.5 mmol) at room temperature. The reaction mixture was stirred for 7 h and then concentrated. The residue was dissolved in CHCl3 (200 mL) and washed with saturated NaHCO3 (2×100 mL). The organic layer was dried over MgSO4, filtered, and concentrated. The residue was purified by column chromatography (silica gel, 90:9:1 CHCl3/CH3OH/NH4OH) to afford Boc-urea 92 (280 mg, 62%) as a light yellow solid: 1H NMR (300 MHz, CD3OD) δ 7.67 (t, J=7.8 Hz, 2H), 7.57 (s, 1H), 7.31 (d, J=8.1 Hz, 1H), 7.19 (s, 2H), 4.18 (t, J=5.4 Hz, 2H), 3.62 (t, J=6.0 Hz, 2H), 2.82 (t, J=6.3 Hz, 2H), 2.12 (t, J=5.7 Hz, 2H), 1.85-1.70 (m, 4H), 1.54 (s, 9H), 1.45 (s, 9H).

Workup

  1. concentrationconcentrated
  2. dissolutionThe residue was dissolved in CHCl3 (200 mL)
  3. washwashed with saturated NaHCO3 (2×100 mL)
  4. dry with materialThe organic layer was dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by column chromatography (silica gel, 90:9:1 CHCl3/CH3OH/NH4OH)

Sources & evidence

ORD record
ord-ea3e8ef5e7fc49d99ad6190078dab93e
Source dataset
uspto-grants-2013_11
Patent number
US08575176B2

Reaction notes

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