Lithium Hydroxide → HCID 22729978, compound

HRID 2356129Notes

Reaction equation

HRID 2356129 reaction equation
[Si]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][C:19]([C:22]([O:24]C)=O)=[CH:18][CH:17]=2)=[C:12]([O:26][CH3:27])[CH:11]=1)(C(C)(C)C)(C)C.[Li+].[OH-].[N+:30]([C:33]1[CH:34]=[C:35]([S:49]([NH2:52])(=[O:51])=[O:50])[CH:36]=[CH:37][C:38]=1[NH:39][CH2:40][CH2:41][S:42][C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1)([O-:32])=[O:31].CCN=C=NCCCN(C)C>C1COCC1.CN(C1C=CN=CC=1)C.C(OCC)(=O)C>[OH:8][CH2:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:17]=[CH:18][C:19]([C:22]([NH:52][S:49]([C:35]3[CH:36]=[CH:37][C:38]([NH:39][CH2:40][CH2:41][S:42][C:43]4[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=4)=[C:33]([N+:30]([O-:32])=[O:31])[CH:34]=3)(=[O:50])=[O:51])=[O:24])=[CH:20][CH:21]=2)=[C:12]([O:26][CH3:27])[CH:11]=1

Participants

8

Reactant 4

HCID 3939Lithium HydroxideHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 8461424HCID 8461424, compoundHCID 68454501HCID 68454501, compound

Product 1

HCID 22729978HCID 22729978, compound

Reagents, catalysts & solvents 3

HCID 142844-(Dimethylamino)pyridineCatalystHCID 8028TetrahydrofuranSolventHCID 8857Ethyl AcetateSolvent

Procedure

A mixture of Example 438A (0.50 mmol) and 1M LiOH (0.60 mL) in THF (2 mL) was heated to 50° C., stirred for 3 hours, concentrated, dissolved in DMF (5 mL), and treated with a mixture of Example 77B (211 mg, 0.60 mmol), EDCI (193 mg, 1.0 mmol), and DMAP (50 mg). The mixture was stirred for 16 hours, treated with 1M HF (3 mL), stirred for 3 hours, diluted with ethyl acetate (100 mL), washed sequentially with 1M HCl (10 mL), water (20 mL), and brine (10 mL), dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 50-100% ethyl acetate/hexanes to provide the desired product. MS (ESI(−)) m/e 592 (M−H)−; 1H NMR (300 MHz, DMSO-d6) δ 8.79 (t, 1H), 8.62 (d, 1H), 7.92 (dd, 1H), 7.89 (d, 2H), 7.54 (d, 2H), 7.37 (m, 2H), 7.28 (r, 3H), 7.18 (tt, 1H), 7.06 (s, 1H), 6.97 (d, 1H), 4.54 (s, 2H), 3.76 (s, 3H), 3.66 (q, 2H), 3.20 (t, 2H).

Workup

  1. concentrationconcentrated
  2. dissolutiondissolved in DMF (5 mL)
  3. stirringThe mixture was stirred for 16 hours
  4. additiontreated with 1M HF (3 mL)
  5. stirringstirred for 3 hours
  6. washwashed sequentially with 1M HCl (10 mL), water (20 mL), and brine (10 mL)
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe concentrate was purified by flash column chromatography on silica gel with 50-100% ethyl acetate/hexanes

Sources & evidence

ORD record
ord-3a8b377eccb349dcbe00d5360e86102f
Source dataset
uspto-grants-2010_07
Patent number
US07754886B2

Reaction notes

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