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Hydrochloric Acid → 6-methyl-3-piperidin-4-yl-thieno[2,3-d]isoxazole Hydrochloride

HRID 501299
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인쇄 미리보기

반응식

HRID 501299 반응식
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[C:18]3[S:19][CH:20]=[C:21]([CH3:22])[C:17]=3[O:16][N:15]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:23]>CO>[ClH:23].[CH3:22][C:21]1[C:17]2[O:16][N:15]=[C:14]([CH:11]3[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]3)[C:18]=2[S:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 588177444-(6-Methyl-thieno[2,3-d]isoxazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 231124496-methyl-3-piperidin-4-yl-thieno[2,3-d]isoxazole Hydrochloride

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Stir a solution of 4-(6-methyl-thieno[2,3-d]isoxazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (8.84 mmol, 2.85 g, 1.00 equivalents) in hydrochloric acid (48.75 mL, 1 M solution in diethyl ether) and methanol (2.00 mL) at room temperature for 3.5 hours. Filter the suspension, collect the white solid and dry to yield the desired product (659 mg). Allow the mother liquor to age overnight, filter, collect the white solid and dry to yield additional desired product (1.252 g). LC/MS (ESI), m/e 223 (MH+), retention time 1.14 minutes. Condition II.

후처리

  1. filtrationFilter the suspension
  2. customcollect the white solid
  3. customdry

출처 및 근거

ORD 기록
ord-1a532aaf8d4047398905385d6f288290
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07772252B2

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