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Hydrochloric Acid → HCID 22273530、化合物

HRID 1064320
ノート
印刷プレビュー

反応式

HRID 1064320 の反応式
[CH3:1][NH:2][S:3]([C:6]1[CH:11]=[CH:10][C:9]([NH2:12])=[CH:8][CH:7]=1)(=[O:5])=[O:4].Cl.CCO[CH2:17][CH3:18].N#CN.[CH3:22][N:23]1[C:27]([C:28]2[CH:33]=[CH:32][N:31]=[C:30](NC3C=CC(S(=O)(=O)N)=CC=3)[N:29]=2)=[CH:26][N:25]=C1.C[O-].[Na+].C(=O)([O-])O.[Na+]>CO.C(#N)C.CC(N(C)C)=O>[CH3:22][N:23]1[C:27]([C:28]2[CH:33]=[CH:32][N:31]=[C:30]([NH:12][C:9]3[CH:10]=[CH:11][C:6]([S:3](=[O:4])(=[O:5])[NH:2][CH3:1])=[CH:7][CH:8]=3)[N:29]=2)=[CH:26][N:25]=[C:17]1[CH3:18]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

11

反応物 7

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 9864CyanamideHCID 743684-amino-N-methylbenzene-1-sulfonamideHCID 516892Sodium BicarbonateHCID 10942334Sodium MethoxideHCID 22273540HCID 22273540、化合物

生成物 1

HCID 22273530
HCID 22273530、化合物
収率 20%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 6342Acetonitrile溶媒HCID 31374Dimethylacetamide溶媒

反応条件

温度
100 °C

実験手順

N-Methyl-4-aminobenzenesulphonamide (Method 110; 250 mg, 1.3 mmol) was dissolved in MeOH (3 ml) and 1M HCl in ether (1.3 ml, 1.3 mmol) added. Cyanamide (68 mg, 1.6 mmol) was added along with DMA (0.5 ml). The mixture was heated to 100° C. for 30 min. To this was added 5-(3-dimethylaminoprop-2-en-1-oyl)-1,2-dimethylimidazole (Method 15; 230 mg, 1.2 mmol) and sodium methoxide (150 mg, 2.6 mmol) and heated to 180° C. for 1 hr. The reaction mixture was poured into sat. sodium hydrogen carbonate solution and the resultant solid collected. The solid was triturated with hot DMF and filtered. The filtrate was evaporated in vacuo and purified by flash chromatography on silica gel eluting with DCM/2% methanolic ammonia (100:0 increasing in polarity to 85:15) to yield a white solid which was digested with acetonitrile to yield the title compound as a solid (84 mg, 20%). NMR: 2.38 (d, 6H), 3.95 (s, 3H), 7.19 (d, 2H), 7.63 (s, 1H), 7.68 (d, 2H), 7.93 (d, 2H), 8.43 (d, 1H), 9.91 (s, 1H); m/z 359.

後処理

  1. temperatureheated to 180° C. for 1 hr
  2. customthe resultant solid collected
  3. customThe solid was triturated with hot DMF
  4. filtrationfiltered
  5. customThe filtrate was evaporated in vacuo
  6. custompurified by flash chromatography on silica gel eluting with DCM/2% methanolic ammonia (100:0 increasing in polarity to 85:15)
  7. customto yield a white solid which

出典と根拠

ORDレコード
ord-240908f8b1034283aa8ee14a69cc62a5
出典データセット
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06969714B2

反応ノート

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