Hydrochloric Acid → HCID 59517550, compound

HRID 1160779Notes

Reaction equation

HRID 1160779 reaction equation
[CH2:1]([C:3]1[N:4]=[C:5]2[CH:10]=[CH:9][C:8]([S:11][CH2:12][CH3:13])=[N:7][N:6]2[C:14]=1[S:15]([NH2:18])(=[O:17])=[O:16])[CH3:2].[CH3:19][O:20][C:21]1[CH:26]=[C:25]([O:27][CH3:28])[N:24]=[C:23]([NH:29][C:30](=O)[O:31]C2C=CC=CC=2)[N:22]=1.C1CCN2C(=NCCC2)CC1.Cl>C(#N)C.O>[CH3:28][O:27][C:25]1[CH:26]=[C:21]([O:20][CH3:19])[N:22]=[C:23]([NH:29][C:30]([NH:18][S:15]([C:14]2[N:6]3[N:7]=[C:8]([S:11][CH2:12][CH3:13])[CH:9]=[CH:10][C:5]3=[N:4][C:3]=2[CH2:1][CH3:2])(=[O:16])=[O:17])=[O:31])[N:24]=1

Participants

7

Procedure

As shown in the above reaction scheme, 2-ethyl-6-ethylthioimidazo[1,2-b]pyridazin-3-ylsulfonamide (0.19 g, 0.66 mmol) and phenyl N-(4,6-dimethoxypyrimidin-2-yl)carbamate (0.20 g, 0.73 mmol) were suspended in acetonitrile (5 ml) and stirred at room temperature, during which DBU (0.11 g, 0.73 mmol) was added thereto. After the mixture was stirred at room temperature for 2 hours, the reaction solution was poured into water (50 ml) and adjusted to pH 2 with dilute hydrochloric acid. The precipitated crystals were collected by filtration, and washed with water and ether in this order. The crystals were dried under reduced pressure to give the title compound as colorless crystals. The yield was 0.18 g (58%), and the melting point was 160 to 165° C. (dec.).

Workup

  1. additionwas added
  2. filtrationThe precipitated crystals were collected by filtration
  3. washwashed with water and ether in this order
  4. customThe crystals were dried under reduced pressure

Sources & evidence

ORD record
ord-c50ebfccaab54aa5a52baf09e142c227
Source dataset
uspto-grants-2010_10
Patent number
US07816526B2

Reaction notes

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