1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 54767811, compound

HRID 1472297Notes

Reaction equation

HRID 1472297 reaction equation
[OH:1][CH:2]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][C:29]([O:31][CH2:32]/[CH:33]=[CH:34]\[CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40])=[O:30])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH2:13]/[CH:14]=[CH:15]\[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])=[O:11].Cl.CN([CH:45](CC)[C:46](O)=[O:47])C.C[CH2:52][N:53]([CH:57](C)C)[CH:54]([CH3:56])C.CCN=C=NCCCN(C)C>ClCCl.CN(C1C=CN=CC=1)C.CO>[CH3:57][N:53]([CH3:52])[CH2:54][CH2:56][CH2:45][C:46]([O:1][CH:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH2:13]/[CH:14]=[CH:15]\[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])=[O:11])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][C:29]([O:31][CH2:32]/[CH:33]=[CH:34]\[CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH3:40])=[O:30])=[O:47]

Participants

8

Reactant 4

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 81531DiisopropylethylamineHCID 58069948HCID 58069948, compoundHCID 717563981394040-12-0

Product 1

HCID 54767811HCID 54767811, compoundYield 62.2%

Reagents, catalysts & solvents 3

HCID 142844-(Dimethylamino)pyridineCatalystHCID 887MethanolSolventHCID 6344DichloromethaneSolvent3×

Procedure

The alcohol 9 (0.083 g, 0.147 mmol) was dissolved in 20 mL of dichloromethane and to it dimethylaminobutyric acid hydrochloride (0.030 g, 0.176 mmol) was added followed by Hunig's base (0.045 g, 0.44 mmol) and DMAP (2 mg). To this mixture EDCI (0.034 g, 0.176 mmol) was added and the reaction mixture was stirred at room temperature overnight and the TLC (silica gel, 10% MeOH in CH2Cl2) showed complete disappearance of the starting alcohol. The reaction mixture was diluted with CH2Cl2 (40 mL) and washed with saturated NaHCO3 (50 mL), water (60 mL) and brine (60 mL). The combined organic layers were dried over anhyd. Na2SO4 and solvents were removed in vacuo. The crude product thus obtained was purified by Combiflash Rf purification system (40 g silicagel, 0-10% MeOH in CH2Cl2) to isolate the pure product (0.062 g, 62%) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 5.74-5.58 (m, 2H), 5.51 (dtt, J=9.7, 6.8, 1.3 Hz, 2H), 4.95-4.75 (m, 1H), 4.61 (d, J=6.8 Hz, 4H), 2.35-2.24 (m, 8H), 2.22 (d, J=7.9 Hz, 6H), 2.09 (q, J=6.9 Hz, 4H), 1.83-1.72 (m, 2H), 1.60 (dd, J=14.4, 7.2 Hz, 4H), 1.49 (d, J=5.7 Hz, 4H), 1.41-1.13 (m, 30H), 0.88 (t, J=6.9 Hz, 6H). 13C NMR (101 MHz, CDCl3) δ 173.72, 173.36, 135.40, 123.35, 74.12, 60.18, 58.95, 45.46, 34.30, 34.11, 32.45, 31.67, 29.38, 29.35, 29.17, 29.07, 28.84, 27.53, 25.28, 24.93, 23.16, 22.59, 14.06. MW calc. for C41H75NO6 (MH+): 678.04. found: 678.5.

Workup

  1. additionwas added
  2. washwashed with saturated NaHCO3 (50 mL), water (60 mL) and brine (60 mL)
  3. customThe combined organic layers were dried over anhyd
  4. customNa2SO4 and solvents were removed in vacuo
  5. customThe crude product thus obtained
  6. customwas purified by Combiflash Rf purification system (40 g silicagel, 0-10% MeOH in CH2Cl2)

Sources & evidence

ORD record
ord-6e88c853275e47eea66b62b36ae850de
Source dataset
uspto-grants-2015_04
Patent number
US09012498B2

Reaction notes

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