1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 21952920, compound

HRID 2215684Notes

Reaction equation

HRID 2215684 reaction equation
[CH:1]1([O:6][C:7]2[CH:8]=[C:9]([C:15]3([C:25]#[N:26])[CH2:20][CH2:19][N:18]([CH2:21][C:22](O)=[O:23])[CH2:17][CH2:16]3)[CH:10]=[CH:11][C:12]=2[O:13][CH3:14])[CH2:5][CH2:4][CH2:3][CH2:2]1.C(N=C=NCCCN(C)C)C.ON1[C:43]2C=CC=[CH:47][C:42]=2[N:41]=N1.[CH3:48][O:49]C(ON)(C)C>C(OCC)(=O)C.CN(C)C=O>[CH3:43][C:42]([NH:41][C:22](=[O:23])[CH2:21][N:18]1[CH2:17][CH2:16][C:15]([C:9]2[CH:10]=[CH:11][C:12]([O:13][CH3:14])=[C:7]([O:6][CH:1]3[CH2:2][CH2:3][CH2:4][CH2:5]3)[CH:8]=2)([C:25]#[N:26])[CH2:20][CH2:19]1)([O:49][CH3:48])[CH3:47]

Participants

7

Procedure

The compound (239 mg) prepared in Example 2, 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC; 192 mg), 1-hydroxybenzotriazole (HOBt; 135 mg), dimethylformamide (4 ml) and (1-methoxy-1-methylethyl)oxyamine (0.35 ml) was stirred at room temperature for 3 hours. The reaction mixture was diluted with ethyl acetate, washed with water (twice), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1→ethyl acetate alone) to thereby obtain the title compound (289 mg) having the following physical properties.

Workup

  1. washwashed with water (twice),
  2. dry with materialdried over anhydrous sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was purified by silica gel column chromatography (hexane

Sources & evidence

ORD record
ord-df03ecf9115047d0a8b9eac569a790fa
Source dataset
uspto-grants-2006_09
Patent number
US07109342B2

Reaction notes

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