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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 23145989, 화합물 → HCID 23145982, 화합물

HRID 13760
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HRID 13760 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([CH2:8][C:9]2[CH:19]=[CH:18][C:12]([C:13]([O:15]CC)=[O:14])=[CH:11][C:10]=2[C:20]([F:23])([F:22])[F:21])[CH2:4][CH2:3]1>CO>[CH3:1][N:2]1[CH2:3][CH2:4][CH:5]([CH2:8][C:9]2[CH:19]=[CH:18][C:12]([C:13]([OH:15])=[O:14])=[CH:11][C:10]=2[C:20]([F:21])([F:23])[F:22])[CH2:6][CH2:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 23145989HCID 23145989, 화합물

생성물 1

HCID 23145982HCID 23145982, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

This compound was prepared in the same manner as in Reference Example 1 (step 6), except that ethyl 4-(1-methylpiperidin-4-ylmethyl)-3-trifluoromethylbenzoate obtained in the step 1 was used, and that the crude product was mixed with methanol and stirred, insolubles were removed by filtration, the filtrate was distilled off under reduced pressure, and then the residue was crystallized by adding acetonitrile.

후처리

  1. customobtained in the step 1
  2. custominsolubles were removed by filtration
  3. distillationthe filtrate was distilled off under reduced pressure
  4. customthe residue was crystallized
  5. additionby adding acetonitrile

출처 및 근거

ORD 기록
ord-566edd5b8b8c4f61ba505a198e9a2476
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728131B2

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