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Pyridine → N-(5-bromothiazol-2-ylcarbamoyl)-5-methylbenzo[b]thiophene-2-sulfonamide

HRID 1009001
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HRID 1009001 반응식
[CH3:1][C:2]1[CH:14]=[CH:13][C:5]2[S:6][C:7]([S:9](Cl)(=[O:11])=[O:10])=[CH:8][C:4]=2[CH:3]=1.[O-:15][C:16]#[N:17].[Na+].N1C=CC=CC=1.Br.[NH2:26][C:27]1[S:28][C:29]([Br:32])=[CH:30][N:31]=1>C(#N)C>[Br:32][C:29]1[S:28][C:27]([NH:26][C:16]([NH:17][S:9]([C:7]2[S:6][C:5]3[CH:13]=[CH:14][C:2]([CH3:1])=[CH:3][C:4]=3[CH:8]=2)(=[O:11])=[O:10])=[O:15])=[N:31][CH:30]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1049PyridineHCID 517096Sodium CyanateHCID 27238485-Bromothiazol-2-amine monohydrobromideHCID 27947715-Methyl-1-benzothiophene-2-sulfonyl chloride

생성물 1

HCID 42634696N-(5-bromothiazol-2-ylcarbamoyl)-5-methylbenzo[b]thiophene-2-sulfonamide수율 78.2%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

실험 절차

To a suspension of 5-methyl-benzo[b]thiophenesulfonyl chloride (Maybridge, CAS: 90273-30-6, 0.37 g) in acetonitrile (5.0 mL) were added sodium cyanate (0.163 g) in one portion and pyridine (0.60 mL). The reaction mixture was stirred at rt for 3 h, then 2-amino-5-bromothiazole hydrobromide (0.286 g) was added in one portion. The mixture was stirred at rt for 4 h and quenched with 70% acetic acid (2.4 mL) and water (4.0 mL). The suspension was filtered, washed with waterlethanol and water, dried over P2O5 under high vacuum to obtain the desired compound (0.372 g) as a creamy solid. MS (ISN): m/e 430.1, 432.0 (M−H)−

후처리

  1. stirringThe mixture was stirred at rt for 4 h
  2. customquenched with 70% acetic acid (2.4 mL) and water (4.0 mL)
  3. filtrationThe suspension was filtered
  4. washwashed with waterlethanol and water
  5. dry with materialdried over P2O5 under high vacuum

출처 및 근거

ORD 기록
ord-79accb4e2e0c4db8b83d899b07c47d1d
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07973051B2

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