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5-(4-Cyanomethyl-phenyl)-thiophene-2-sulfonic acid tert-butylamide → 5-(4-Cyanomethyl-phenyl)-thiophene-2-sulfonic acid amide

HRID 1696757
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HRID 1696757 반응식
C([NH:5][S:6]([C:9]1[S:10][C:11]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][C:21]#[N:22])=[CH:16][CH:15]=2)=[CH:12][CH:13]=1)(=[O:8])=[O:7])(C)(C)C>C(O)(C(F)(F)F)=O>[C:21]([CH2:20][C:17]1[CH:16]=[CH:15][C:14]([C:11]2[S:10][C:9]([S:6]([NH2:5])(=[O:7])=[O:8])=[CH:13][CH:12]=2)=[CH:19][CH:18]=1)#[N:22]
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참가 물질

3

반응물 1

HCID 672735715-(4-Cyanomethyl-phenyl)-thiophene-2-sulfonic acid tert-butylamide

생성물 1

HCID 672744645-(4-Cyanomethyl-phenyl)-thiophene-2-sulfonic acid amide수율 73%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

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온도
50 °C

실험 절차

5-(4-Cyanomethyl-phenyl)-thiophene-2-sulfonic acid tert-butylamide (260 mg) was suspended in TFA (10 mL) and stirred 2 h at 50° C. The mixture was evaporated to dryness and trituated with toluene (2 mL). The obtained precipitate was filtered off, washed with toluene and dried in vacuo to yield 5-(4-Cyanomethyl-phenyl)-thiophene-2-sulfonic acid amide (157 mg, 73%) as a white solid.

후처리

  1. customThe mixture was evaporated to dryness
  2. filtrationThe obtained precipitate was filtered off
  3. washwashed with toluene
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-4b49f9f63d2c48edac2a20c8d2cfb593
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163778B2

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