Triethylamine → 5-Methyl-thiophene-2-carboxylic acid (5-methoxy-7-phenyl-benzothiazol-2-yl)-amide

HRID 1060280Notes

Reaction equation

HRID 1060280 reaction equation
[NH2:1][C:2]1[S:3][C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[CH:9][C:8]([O:17][CH3:18])=[CH:7][C:5]=2[N:6]=1.C(N([CH2:24][CH3:25])CC)C.[OH-:26].[Na+]>ClCCl>[CH3:18][O:17][C:8]1[CH:9]=[C:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:4]2[S:3][C:2]([NH:1][C:10]([C:4]3[S:3][C:24]([CH3:25])=[CH:7][CH:5]=3)=[O:26])=[N:6][C:5]=2[CH:7]=1

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 14798Sodium HydroxideHCID 222831342-Amino-5-methoxy-7-phenylbenzothiazol

Product 1

HCID 865849155-Methyl-thiophene-2-carboxylic acid (5-methoxy-7-phenyl-benzothiazol-2-yl)-amideYield 5%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

2-Amino-5-methoxy-7-phenylbenzothiazol (45 mg, 0.18 mmol) is dissolved in dichloromethane (2 ml) and subsequently treated with triethylamine (0.073 ml, 0.53 mmol) and 5-methyll-thiophene-2-carbonyl chloride (56 mg, 0.35 mmol). After 6 h, further 0.073 ml, 0.53 mmol) and 5-methyll-thiophene-2-carbonyl chloride (56 mg, 0.35 mmol) are added and the mixture is stirred for additional 18 h at ambient. After addition of 0.1M aqueous sodium hydroxide, the mixture is stirred for additional 16 h. The organic layer is separated, dried and evaporated to dryness. Flash chromatography (silica, eluent ethyl acetate/cyclohexane 1:1, containing 0.5% of 25% aqueous ammonia) affords (10 mg, 5%) of the product as white solid. MS: m/e=380 (M+).

Workup

  1. stirringthe mixture is stirred for additional 16 h
  2. customThe organic layer is separated
  3. customdried
  4. customevaporated to dryness
  5. additionFlash chromatography (silica, eluent ethyl acetate/cyclohexane 1:1, containing 0.5% of 25% aqueous ammonia)

Sources & evidence

ORD record
ord-17dd2c60bc484cbd8a3048fe632b7dc2
Source dataset
uspto-grants-2003_02
Patent number
US06521754B2

Reaction notes

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