Triethylamine → 5-amino-3-(3-bromobenzyl)-1-isopropyl-1H-pyrazole-4-carbonitrile

HRID 530972

반응식

HRID 530972 반응식
CO[C:3]([CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([Br:16])[CH:11]=1)=[C:4]([C:7]#[N:8])[C:5]#[N:6].Cl.[CH:18]([NH:21][NH2:22])([CH3:20])[CH3:19].C(N(CC)CC)C>C(O)C>[NH2:6][C:5]1[N:21]([CH:18]([CH3:20])[CH3:19])[N:22]=[C:3]([CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([Br:16])[CH:11]=2)[C:4]=1[C:7]#[N:8]

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 855731-Isopropylhydrazine hydrochlorideHCID 716059322-(Methoxy(3-bromobenzyl)methylene)malononitrile

생성물 1

HCID 895873135-amino-3-(3-bromobenzyl)-1-isopropyl-1H-pyrazole-4-carbonitrile수율 87.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Compound 33 (3.124 g, 11.3 mmol), isopropylhydrazine hydrochloride (1.27 g, 11.5 mmol) (purchased from Ryan Scientific) and triethylamine (6.40 mL, 46.0 mmol) were allowed to react in ethanol (75 mL) at room temperature for 1 hr. After concentrating the reaction mixture, it was purified by silica chromatography using a chloroform/methanol solvent system (methanol gradient increased with time from 0-10%). The relevant fractions were concentrated in vacuo to yield a yellow powder (3.15 g, 87% yield): 1H NMR (400 MHz, DMSO) δ 7.41 (m, 2H), 7.26 (td, J=7.7, 1.2, 1H), 7.21 (dt, J=7.7, 1.3, 1H), 6.50 (s, 2H), 4.38 (hept, J=6.5, 1H), 3.81 (s, 2H), 1.27 (d, J=6.5, 6H); 13C NMR (100 MHz, DMSO) δ 151.01, 150.15, 141.24, 131.05, 130.53, 129.16, 127.45, 121.55, 115.16, 71.77, 47.24, 32.88, 21.35; [M+H]+ calculated for C14H15BrN4 319.0, 321.0 found 318.9: 321.0.

후처리

  1. concentrationAfter concentrating the reaction mixture, it
  2. customwas purified by silica chromatography
  3. temperaturea chloroform/methanol solvent system (methanol gradient increased with time from 0-10%)
  4. concentrationThe relevant fractions were concentrated in vacuo

출처 및 근거

ORD 기록
ord-bb03d74923ac4bddba44e2bc80cbf309
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09353116B2

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