Diisopropylethylamine → N-{[(2S)-4-(2,3-dichlorobenzyl)morpholin-2-yl]methyl}-N'-prop-2-ynylurea

HRID 1371449Notes

Reaction equation

HRID 1371449 reaction equation
[CH2:1]([NH:4][C:5](=O)[O:6]C1C=CC([N+]([O-])=O)=CC=1)[C:2]#[CH:3].[Cl:17][C:18]1[C:32]([Cl:33])=[CH:31][CH:30]=[CH:29][C:19]=1[CH2:20][N:21]1[CH2:26][CH2:25][O:24][C@@H:23]([CH2:27][NH2:28])[CH2:22]1.C(N(CC)C(C)C)(C)C>ClCCl>[Cl:17][C:18]1[C:32]([Cl:33])=[CH:31][CH:30]=[CH:29][C:19]=1[CH2:20][N:21]1[CH2:26][CH2:25][O:24][C@@H:23]([CH2:27][NH:28][C:5]([NH:4][CH2:1][C:2]#[CH:3])=[O:6])[CH2:22]1

Participants

5

Procedure

A solution of Intermediate 22 (0.024 g) in dichloromethane (1 ml) was stirred with Intermediate 20 (0.033 g) and N,N-diisopropylethylamine (0.022 ml) for 3 h at 23° C. The solvent was removed in vacuo and the residue was purified by solid phase extraction (Isolute SCX sulphonic acid column) eluting with methanol followed by 10% 0.880 ammonia solution in methanol. The basic fraction was concentrated in vacuo, and the residue was dissolved in dichloromethane (5 ml), and the solution shaken with polystyrene methyl isocyanate resin (Argonaut technologies, 0.256 g, 1.43 mmol/g) for 16 h. The solution Was drained from the resin and the resin washed with dichloromethane (8 ml); the combined filtrate and washings were concentrated in vacuo to give the title compound as a pale yellow gum (0.02 g).

Workup

  1. customThe solvent was removed in vacuo
  2. customthe residue was purified by solid phase extraction (Isolute SCX sulphonic acid column)
  3. washeluting with methanol
  4. concentrationThe basic fraction was concentrated in vacuo
  5. dissolutionthe residue was dissolved in dichloromethane (5 ml)
  6. washthe resin washed with dichloromethane (8 ml)
  7. concentrationthe combined filtrate and washings were concentrated in vacuo

Sources & evidence

ORD record
ord-e36ede6d838840ebaf43c9322f13bf2c
Source dataset
uspto-grants-2007_01
Patent number
US07157457B2

Reaction notes

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