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Sodium Carbonate → 4-(7-Chloro-4-quinolylamino)-N-(1-n-butyl-4-piperidyl)-benzene sulphonamide

HRID 1580685
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HRID 1580685 반응식
Cl.[Cl:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7]([NH:13][C:14]3[CH:19]=[CH:18][C:17]([S:20](Cl)(=[O:22])=[O:21])=[CH:16][CH:15]=3)=[CH:8][CH:9]=[N:10]2)=[CH:5][CH:4]=1.[NH2:24][CH:25]1[CH2:30][CH2:29][N:28]([CH2:31][CH2:32][CH2:33][CH3:34])[CH2:27][CH2:26]1.C(=O)([O-])[O-].[Na+].[Na+]>O.C(Cl)(Cl)Cl>[Cl:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7]([NH:13][C:14]3[CH:19]=[CH:18][C:17]([S:20]([NH:24][CH:25]4[CH2:30][CH2:29][N:28]([CH2:31][CH2:32][CH2:33][CH3:34])[CH2:27][CH2:26]4)(=[O:22])=[O:21])=[CH:16][CH:15]=3)=[CH:8][CH:9]=[N:10]2)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 10340Sodium CarbonateHCID 122628201-Butylpiperidin-4-amineHCID 201495884-(7-Chloro-4-quinolinylamino)benzenesulphonyl chloride hydrochloride

생성물 1

HCID 215635394-(7-Chloro-4-quinolylamino)-N-(1-n-butyl-4-piperidyl)-benzene sulphonamide

시약·촉매·용매 2

HCID 962Water용매
HCID 6212
Chloroform
용매

실험 절차

7.8 Grams of 4-(7-chloro-4-quinolylamino)-benzenesulphonyl chloride hydrochloride [prepared as in Example 1(b)] were added in portions to a stirred mixture of 3.13 grams of 4-amino-1-n-butyl piperidine and 21.2 grams of sodium carbonate in 50 milliliters of water and 50 milliliters of chloroform. After stirring overnight at room temperature, the chloroform layer was separated, washed with water, dried and evaporated to give a brown solid which was triturated with ether to give 5.0 grams of the title compound as the hemihydrate. Melting point 190°-191°C.

후처리

  1. customthe chloroform layer was separated
  2. washwashed with water
  3. customdried
  4. customevaporated
  5. customto give a brown solid which
  6. customwas triturated with ether

출처 및 근거

ORD 기록
ord-d6aa4defd9224e9ea4848a140121ca2f
출처 데이터셋
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03933829

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