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1-Piperidinecarboxaldehyde → 8-Chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carbonyl chloride

HRID 577435
ノート
印刷プレビュー

反応式

HRID 577435 の反応式
C(N1CCCCC1)=O.S(Cl)(Cl)=O.[Cl:13][C:14]1[C:15]2[N:16]([CH:24]=[C:25]([C:27]([OH:29])=O)[N:26]=2)[CH:17]=[C:18]([C:20]([F:23])([F:22])[F:21])[CH:19]=1.COC(C1N=C2C([Cl:42])=CC(C(F)(F)F)=CN2C=1)=O>CO.C1(C)C=CC=CC=1>[Cl:13][C:14]1[C:15]2[N:16]([CH:24]=[C:25]([C:27]([Cl:42])=[O:29])[N:26]=2)[CH:17]=[C:18]([C:20]([F:23])([F:22])[F:21])[CH:19]=1
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

7

反応物 4

HCID 174291-PiperidinecarboxaldehydeHCID 24386Thionyl ChlorideHCID 39288178-Chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid2 回HCID 867296498-Chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid methyl ester

生成物 1

HCID 867296488-Chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carbonyl chloride

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 1140Toluene溶媒

反応条件

温度
90 °C

実験手順

To a 3000 mL three-neck round bottom flask equipped with an overhead stirrer, thermo pocket, addition funnel and nitrogen tube was charged toluene (1000 mL), N-formyl piperidine (3.54 g, 0.031 mol) and thionyl chloride (67 g, 0.559 moles) at 23° C. under nitrogen atmosphere. The resultant reaction mass was heated to 82° C. and to this 8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid (100 g, 0.373 moles) (prepared as in WO 2010/129500) was charged lot wise (5 lots) over a period of 60 min. The walls of the reactor were rinsed with 500 mL toluene. After addition, the resultant reaction mass was stirred at 90° C. for 75 min and the progress of the reaction was monitored by HPLC. For this, 0.5 mL of the reaction mass was diluted with 3 mL of methanol and the formation of acid chloride was analyzed indirectly by detecting its corresponding methyl ester by HPLC). After 2 hours, HPLC analysis indicated about 0.35 a % of unreacted 8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid and about 99.0 a % of 8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid methyl ester. The resultant reaction mass was further heated to 140° C. (oil bath temperature) and distilled at about 109° C. (mass temperature) and 105-107° C. (vapor temperature) at atmospheric pressure over a period of 2.5 hours to remove toluene (about 600 mL) and excess thionyl chloride present in the reaction mass. After distillation, the reaction mass was gradually cooled to 30° C. over a period of 60 min. The concentration of 8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid was about 0.07 a % and the concentration of 8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid methyl ester about 99.2 a % as measured by HPLC at 230 nm.

後処理

  1. customTo a 3000 mL three-neck round bottom flask equipped with an overhead stirrer
  2. additionthermo pocket, addition funnel and nitrogen tube
  3. customThe resultant reaction mass
  4. additionwas charged lot wise (5 lots) over a period of 60 min
  5. washThe walls of the reactor were rinsed with 500 mL toluene
  6. additionAfter addition
  7. customthe resultant reaction mass
  8. waitAfter 2 hours
  9. customThe resultant reaction mass
  10. temperaturewas further heated to 140° C. (oil bath temperature)
  11. distillationdistilled at about 109° C. (mass temperature) and 105-107° C. (vapor temperature) at atmospheric pressure over a period of 2.5 hours
  12. customto remove toluene (about 600 mL) and excess thionyl chloride present in the reaction mass
  13. distillationAfter distillation
  14. temperaturethe reaction mass was gradually cooled to 30° C. over a period of 60 min

出典と根拠

ORDレコード
ord-f8d99cb9a9504af39fd3737c45a46686
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09040554B2

反応ノート

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