Dimethyl Sulfoxide → 5-Methyl-4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carbaldehyde

HRID 2216585ノート

反応式

HRID 2216585 の反応式
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH3:11][N:12]1[CH2:17][CH2:16][C:15]2[S:18][C:19]([CH2:21][OH:22])=[CH:20][C:14]=2[CH2:13]1.C(N(CC)CC)C>C(Cl)Cl>[CH3:11][N:12]1[CH2:17][CH2:16][C:15]2[S:18][C:19]([CH:21]=[O:22])=[CH:20][C:14]=2[CH2:13]1

参加物

6

反応条件

温度
50 °C

実験手順

DMSO (1.7 ml, 24 mmol) in 5 ml CH2Cl2 was cooled to −50–60° C. Oxalyl chloride (1 ml, 11 mmol) in 20 ml DCM was then added within 5 minutes at 50° C. The mixture was kept at −50° C. for 5 minutes and then 1.67 gram (9 mmol) of (5-Methyl-4,5,6,7-tetrahydro-thieno[3,2-c]pyridin-2-yl)-methanol in 20 ml DCM was added at 50° C. and the mixture was stirred for another 15 minutes at 50° C. Triethylamine (7 ml) was then added at −50° C. and after 5 minutes the bath was removed and the mixture is naturally warmed up to 23° C. It was washed with 100 ml water and extracted with 100 ml ethyl acetate. The combined organic layers were dried over magnesium sulfate. Filter. Concentrate and flash column chromatograph using 0–15% methanol in ethyl acetate yielded 736 mg (45% yield) product.

後処理

  1. customwas removed
  2. temperaturethe mixture is naturally warmed up to 23° C
  3. washIt was washed with 100 ml water
  4. extractionextracted with 100 ml ethyl acetate
  5. dry with materialThe combined organic layers were dried over magnesium sulfate
  6. filtrationFilter
  7. concentrationConcentrate

出典と根拠

ORDレコード
ord-47c39d0311c4406ea520ad0b1472fdac
出典データセット
uspto-grants-2006_09
特許番号
US07112582B2

反応ノート

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