Triethylamine → N-(6-fluoro-1,3-benzothiazol-2-yl)-2,2,3,3-tetramethylcyclopropanecarboxamide

HRID 1037839Notes

Reaction equation

HRID 1037839 reaction equation
[F:1][C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7]([NH2:9])[S:8][C:4]=2[CH:3]=1.CCN=C=NCCCN(C)C.Cl.C(N(CC)CC)C.[CH3:31][C:32]1([CH3:40])[C:34]([CH3:36])([CH3:35])[CH:33]1[C:37](O)=[O:38]>CCOC(C)=O.C1COCC1.CCN(CC)CC>[F:1][C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7]([NH:9][C:37]([CH:33]3[C:34]([CH3:36])([CH3:35])[C:32]3([CH3:40])[CH3:31])=[O:38])[S:8][C:4]=2[CH:3]=1

Participants

7

Procedure

A mixture of 6-fluoro-benzothiazol-2-ylamine (1 equiv), N-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride (1 equiv), 1-hydroxybenzotniazole, triethylamine (1.1 equiv), and 2,2,3,3-tetramethylcyclopropanecarboxylic acid (0.8 equiv) in 3:1 THF/Et3N (1 M) and were stirred overnight at room temperature. The mixture was diluted with EtOAc, washed with 1 M aqueous NaHCO3, dried (Na2SO4), filtered, and concentrated. Puried by silica gel chromatography afforded the title compound. MS (ESI+) m/z 293 (M+H)+.

Workup

  1. washwashed with 1 M aqueous NaHCO3
  2. dry with materialdried (Na2SO4)
  3. filtrationfiltered
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-937f787010a241869229a48284db1539
Source dataset
uspto-grants-2013_10
Patent number
US08546583B2

Reaction notes

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