4-chloro-N-methoxy-N-methyl-3-sulfamoyl-benzamide → 2-Chloro-5-[4-(3-methyl-piperidin-1-yl)-benzoyl]-benzenesulfonamide

HRID 1810185노트

반응식

HRID 1810185 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][CH2:11][CH:10]([CH3:14])[CH2:9]2)=[CH:4][CH:3]=1.[Cl:15][C:16]1[CH:27]=[CH:26][C:19]([C:20](N(OC)C)=[O:21])=[CH:18][C:17]=1[S:28](=[O:31])(=[O:30])[NH2:29].C([Li])(C)(C)C>O1CCCC1>[Cl:15][C:16]1[CH:27]=[CH:26][C:19]([C:20](=[O:21])[C:2]2[CH:7]=[CH:6][C:5]([N:8]3[CH2:13][CH2:12][CH2:11][CH:10]([CH3:14])[CH2:9]3)=[CH:4][CH:3]=2)=[CH:18][C:17]=1[S:28]([NH2:29])(=[O:31])=[O:30]

참가 물질

5

반응물 3

HCID 581073994-chloro-N-methoxy-N-methyl-3-sulfamoyl-benzamideHCID 668503451-(4-Bromo-phenyl)-3-methyl-piperidineHCID 178418306HCID 178418306, 화합물

생성물 1

HCID 581074352-Chloro-5-[4-(3-methyl-piperidin-1-yl)-benzoyl]-benzenesulfonamide

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 0.821 g of 1-(4-bromo-phenyl)-3-methyl-piperidine in tetrahydrofuran is cooled to −78° C. and treated with 0.3 g of 4-chloro-N-methoxy-N-methyl-3-sulfamoyl-benzamide. The mixture is stirred for 10 min and treated slowly with 4.31 mL of a solution of tert-butyl lithium (1.5 M) in tetrahydrofuran (3 mL). The orange solution is stirred at −78° C. for 15 min then at 0° C. for 1 hour. The reaction mixture is quenched with saturated aqueous ammonium chloride (100 mL) and extracted with ethyl acetate (2×50 mL). The organics are washed with water, a saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated in vacuo. The residue is loaded on Celite and purified by silica gel chromatography (1:1 hexanes/ethyl acetate) to give 2-chloro-5-[4-(3-methyl-piperidin-1-yl)-benzoyl]-benzenesulfonamide as a light yellow syrup. MS (m/z): 393 (M+1). HPLC Reverse Phase (Nucleosil 100-5 C18, gradient 10->100% CH3CN in 5 min) room temperature=5.40 minutes.

후처리

  1. stirringThe orange solution is stirred at −78° C. for 15 min
  2. waitat 0° C. for 1 hour
  3. customThe reaction mixture is quenched with saturated aqueous ammonium chloride (100 mL)
  4. extractionextracted with ethyl acetate (2×50 mL)
  5. washThe organics are washed with water
  6. dry with materiala saturated sodium chloride solution, dried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. custompurified by silica gel chromatography (1:1 hexanes/ethyl acetate)

출처 및 근거

ORD 기록
ord-ca5d1d0f40cb4c2bbf64b55b6e7741e5
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08362063B2

반응 노트

불러오는 중…