Phenethylamine → N-phenethyl 4-benzyloxy-1-methyl-1H-indole-2-carboxyamide
반응식
[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][CH:15]=[C:14]2[C:10]=1[CH:11]=[C:12]([C:19](O)=O)[N:13]2[CH3:18])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN([C:25]([O:29]N1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.C1C=CC2N(O)N=NC=2C=1.CCN(C(C)C)C(C)C.[CH2:63]([NH2:71])[CH2:64][C:65]1[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=1>CN(C=O)C>[CH2:63]([NH:71][C:25]([CH2:19][C:12]1[N:13]([CH3:18])[C:14]2[C:10]([CH:11]=1)=[C:9]([O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[CH:17]=[CH:16][CH:15]=2)=[O:29])[CH2:64][C:65]1[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=1참가 물질
7
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 4-benzyloxy-1-methyl-1H-indole-2-carboxylic acid (0.20 g) in DMF (10 mL) was added TBTU (0.23 g), HOBt (0.11 g) and DIEA (0.27 mL). After 5 min., phenethylamine (0.11 mL) was added and stirring was continued overnight under nitrogen at room temperature. The residue remaining after DMF evaporation was dissolved in EtOAc; washed with dilute HCl, saturated NaHCO3, and brine; dried over MgSO4; and concentrated at reduced pressure to give the intermediate product N-phenethyl 4-benzyloxy-1-methyl-1H-indole-2-carboxyamide (0.18 g) which was used without further purification. Hydrogenation of this product by a method analogous to that described in Example 9 give 0.14 g of the title compound.
후처리
- waitwas continued overnight under nitrogen at room temperature
- customafter DMF evaporation
- dissolutionwas dissolved in EtOAc
- washwashed with dilute HCl, saturated NaHCO3, and brine
- dry with materialdried over MgSO4
- concentrationand concentrated at reduced pressure
출처 및 근거
- ORD 기록
- ord-d32f939899cb4a6bb5e5065127b0b33e
- 출처 데이터셋
- uspto-grants-2008_07
- 특허 번호
- US07402604B2
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