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Sodium Acetate → 4-(2-Amino-thiazol-4-yl)-N-cyclopentyl-benzenesulfonamide

HRID 737194
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반응식

HRID 737194 반응식
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([NH:14][CH:15]2[CH2:19][CH2:18][CH2:17][CH2:16]2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)=O.[NH2:20][C:21]([NH2:23])=[S:22].CC([O-])=O.[Na+]>CCO>[NH2:23][C:21]1[S:22][CH:2]=[C:3]([C:5]2[CH:10]=[CH:9][C:8]([S:11]([NH:14][CH:15]3[CH2:19][CH2:18][CH2:17][CH2:16]3)(=[O:13])=[O:12])=[CH:7][CH:6]=2)[N:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 517045Sodium AcetateHCID 2723790ThioureaHCID 866164394-(2-Bromo-acetyl)-N-cyclopentyl-benzenesulfonamide

생성물 1

HCID 866164404-(2-Amino-thiazol-4-yl)-N-cyclopentyl-benzenesulfonamide

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

4-(2-Bromo-acetyl)-N-cyclopentyl-benzenesulfonamide (150 mg, 0.43 mmol) was combined with thiourea (33 mg, 0.43 mmol) in 7 ml of dry EtOH. To this solution was added NaOAc (53 mg, 0.65 mmol). Reaction mixture was stirred at room temperature for 4 hours. Reaction mixture was evaporated to dryness and used in the next step without further purification.

후처리

  1. customReaction mixture
  2. customReaction mixture
  3. customwas evaporated to dryness
  4. customused in the next step without further purification

출처 및 근거

ORD 기록
ord-e21784417c9c4729b6dea077530b1a9f
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07595398B2

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