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Trifluoroacetic acid → HCID 67461567, 화합물

HRID 2043785
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HRID 2043785 반응식
FC(F)(F)C(O)=O.[CH2:8]([O:10][C:11]([C:13]1[CH:17]=[N:16][N:15](C2CCN(C(OC(C)(C)C)=O)CC2)[N:14]=1)=[O:12])[CH3:9].C(OC(C1N([CH:41]2[CH2:46][CH2:45][N:44](C(OC(C)(C)C)=O)[CH2:43][CH2:42]2)N=NC=1)=O)C>>[N:44]1([C:13]2([C:11]([O:10][CH2:8][CH3:9])=[O:12])[CH:17]=[N:16][NH:15][NH:14]2)[CH2:45][CH2:46][CH2:41][CH2:42][CH2:43]1
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참가 물질

4

반응물 3

HCID 6422Trifluoroacetic acidHCID 67462532HCID 67462532, 화합물HCID 67462944HCID 67462944, 화합물

생성물 1

HCID 67461567HCID 67461567, 화합물

실험 절차

Trifluoroacetic acid (3 mL) was added to 1,1-dimethylethyl 4-[4-(ethoxycarbonyl)-2H-1,2,3-triazol-2-yl]-1-piperidinecarboxylate (0.41 g, 1.3 mmol) (i.e. the product of Example 32, Step A). The reaction mixture was stirred for 45 minutes. The reaction mixture was then concentrated in vacuo. The resulting mixture was treated with saturated aqueous sodium bicarbonate and the aqueous layer was extracted three times with dichloromethane. The solvent was removed with a rotary evaporator to afford 0.23 g of ethyl 4-piperidinyl-2H-1,2,3-triazole-4-carboxylate as an oil. This compound was of sufficient purity to use in subsequent reactions.

후처리

  1. concentrationThe reaction mixture was then concentrated in vacuo
  2. additionThe resulting mixture was treated with saturated aqueous sodium bicarbonate
  3. extractionthe aqueous layer was extracted three times with dichloromethane
  4. customThe solvent was removed with a rotary evaporator

출처 및 근거

ORD 기록
ord-98c55d7d55f1405d8b3e1862e43c6597
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08586611B2

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