2-Aminoadamantane hydrochloride → N-(adamantane-2-yl)-1-(2-nitrophenylsulfonamido)cyclobutanecarboxyamide

HRID 1519079노트

반응식

HRID 1519079 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10]([NH:13][C:14]1([C:18](O)=O)[CH2:17][CH2:16][CH2:15]1)(=[O:12])=[O:11])([O-:3])=[O:2].Cl.[CH:22]12[CH2:31]C3[CH2:27][CH:28]([CH2:30]C(C3)[CH:23]1N)[CH2:29]2.F[P-](F)(F)(F)(F)F.N1([O:49][P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.CC[N:62]([CH:66]([CH3:68])[CH3:67])[CH:63](C)C>C(Cl)Cl>[CH:68]12[CH2:31][CH:22]3[CH2:29][CH:28]([CH2:30][CH:67]([CH2:23]3)[CH:66]1[NH:62][C:63]([CH2:18][C:14]1([NH:13][S:10]([C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=3[N+:1]([O-:3])=[O:2])(=[O:11])=[O:12])[CH2:15][CH2:16][CH2:17]1)=[O:49])[CH2:27]2

참가 물질

6

실험 절차

In a 10-mL flask, 1-(2-nitrophenylsulfonamido)cyclobutanecarboxylic acid (200 mg, 0.666 mmol), 2-adamantanamine hydrochloride (150 mg, 0.799 mmol), and BOP (295 mg, 0.667 mmol) were charged, and CH2Cl2 (3 ml) was charged, followed by stirring for 30 minutes at room temperature. DIPEA (0.28 ml, 1.60 mmol) was added thereto, followed by stirring at room temperature for 12 hours. After the reaction was completed, the organic layer was separated using CH2Cl2 and H2O, dried with MgSO4, and filtered. The resultant mixture was purified with column chromatography (EA/n-Hex=1:2) to obtain N-(adamantane-2-yl)-1-(2-nitrophenylsulfonamido)cyclobutanecarboxyamide (282 mg, 97%).

후처리

  1. stirringby stirring at room temperature for 12 hours
  2. customthe organic layer was separated
  3. dry with materialdried with MgSO4
  4. filtrationfiltered
  5. customThe resultant mixture was purified with column chromatography (EA/n-Hex=1:2)

출처 및 근거

ORD 기록
ord-67341d6b541d45e68a8f5098cf883529
출처 데이터셋
uspto-grants-2015_07
특허 번호
US09073830B2

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