홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Bisulfite → HCID 178429876, 화합물

HRID 1047571
노트
인쇄 미리보기

반응식

HRID 1047571 반응식
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9]([CH:13]1[CH2:18][CH2:17][CH2:16][CH2:15][O:14]1)[N:8]=[C:7]2[CH:19]=O)([O-:3])=[O:2].[CH3:21][CH:22]1[CH2:27][N:26]([C:28]2[CH:29]=[C:30]([NH2:35])[C:31]([NH2:34])=[CH:32][CH:33]=2)[CH2:25][CH2:24][O:23]1.S(=O)(O)[O-].[Na+]>C1COCC1.Cl.C(OCC)(=O)C>[CH3:21][CH:22]1[O:23][CH2:24][CH2:25][N:26]([C:28]2[CH:33]=[CH:32][C:31]3[NH:34][C:19]([C:7]4[C:6]5[C:10](=[CH:11][CH:12]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=5)[N:9]([CH:13]5[CH2:18][CH2:17][CH2:16][CH2:15][O:14]5)[N:8]=4)=[N:35][C:30]=3[CH:29]=2)[CH2:27]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 23665763Sodium BisulfiteHCID 683850274-(2-Methylmorpholino)benzene-1,2-diamineHCID 866732115-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde

생성물 1

HCID 178429876HCID 178429876, 화합물수율 55.5%

시약·촉매·용매 3

HCID 313Hydrochloric Acid촉매
HCID 8028
Tetrahydrofuran
용매
HCID 8857Ethyl Acetate용매

반응 조건

온도
70 °C

실험 절차

5-Nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carbaldehyde (150 mg, 0.545 mmol) and 4-(2-methylmorpholino)benzene-1,2-diamine (113 mg, 0.545 mmol) were dissolved in THF (10 mL) and 2N HCl (1 drop) was added. The solution was heated at a gentle reflux for 30 min. Then, 1N sodium bisulfite (104 mg, 1 mmol; 2 mL of a 1N solution) was added and heated at reflux (70° C.) overnight. The solution was cooled to room temperature, and diluted with ethyl acetate (40 mL). The mixture was washed with water and brine, dried over Na2SO4, and concentrated. Purification by flash chromatography (5% CH3OH/CH2Cl2) afforded the title compound (140 mg). 1H NMR: (400 MHz, CDCl3): δ 9.56 (d, 1H, J=1.6 Hz), 8.28 (m, 1H), 7.74 (d, 1H, J=8.8 Hz), 7.64 (m, 1H), 7.36 (m, 1H), 7.03-6.96 (m, 1H), 5.75 (dd, 1H, J=2.8 and 6.4 Hz), 3.99 (m, 2H), 3.79 (m, 3H), 3.38 (m, 2H), 2.84 (m, 1H), 2.51 (m, 2H), 2.11 (m, 2H), 1.86 (m, 1H), 1.74 (m, 2H), 1.22 (d, 3H, J=6.4 Hz).

후처리

  1. temperatureThe solution was heated at
  2. temperaturea gentle reflux for 30 min
  3. temperatureheated
  4. temperatureThe solution was cooled to room temperature
  5. washThe mixture was washed with water and brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customPurification by flash chromatography (5% CH3OH/CH2Cl2)

출처 및 근거

ORD 기록
ord-328a7e4ea1074e7eb8da8750dcb862c4
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08569511B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트