Trifluoroacetic acid → HCID 178457231, 화합물

HRID 25583

반응식

HRID 25583 반응식
C(O[C:6](=O)[N:7]([C@H:9]1[CH2:14][CH2:13][C@H:12]([C:15]#[C:16][CH2:17][N:18]([CH2:20][CH:21]=[CH2:22])[CH3:19])[CH2:11][CH2:10]1)C)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH2:20]([N:18]([CH3:19])[CH2:17][C:16]#[C:15][C@H:12]1[CH2:13][CH2:14][C@H:9]([NH:7][CH3:6])[CH2:10][CH2:11]1)[CH:21]=[CH2:22]

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 178457235HCID 178457235, 화합물

생성물 1

HCID 178457231HCID 178457231, 화합물수율 107.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 200 mg (0.62 mmol) of trans-{4-[3-(Allyl-methyl-amino)-prop-1-ynyl]-cyclohexyl}-methyl-carbamic acid tert-butyl ester in 3.5 ml CH2Cl2 was treated at 0° C. with 1.7 ml TFA (for 20 min). After 30 min at this temperature, the reaction mixture was evaporated, treated with 1 N NaOH/CH2Cl2 (3×). The organic phase was dried over Na2SO4 and evaporated to yield 147 mg (quantitative) of trans-{4-[3-(Allyl-methyl-amino)-prop-1-ynyl]-cyclohexyl}-methyl-amine, MS: 221 (MH+).

후처리

  1. customthe reaction mixture was evaporated
  2. additiontreated with 1 N NaOH/CH2Cl2 (3×)
  3. dry with materialThe organic phase was dried over Na2SO4
  4. customevaporated

출처 및 근거

ORD 기록
ord-581b627cf2ae4cea946383d4cc2d58e3
출처 데이터셋
uspto-grants-2005_02
특허 번호
US06858651B2

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