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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 14077945, 화합물 → HCID 67481674, 화합물

HRID 2273035
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HRID 2273035 반응식
[N+:1]([CH:4]1[CH:19]([OH:20])[CH:8]2[O:9][CH:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[O:11][CH2:12][CH:7]2[CH2:6][CH:5]1[OH:21])([O-])=O>CO.[NH4+].[OH-].[Ni]>[NH2:1][CH:4]1[CH:19]([OH:20])[CH:8]2[O:9][CH:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[O:11][CH2:12][CH:7]2[CH2:6][CH:5]1[OH:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 14077945HCID 14077945, 화합물

생성물 1

HCID 67481674HCID 67481674, 화합물수율 81%

시약·촉매·용매 3

HCID 935Nickel촉매HCID 887Methanol용매HCID 14923Ammonium Hydroxide용매

실험 절차

To a solution of rac-(2R,4aR,6R,7S,8R,8aR)-7-nitro-2-phenylhexahydro-4H-benzo[d][1,3]dioxine-6,8-diol (Carb. Res. 2002, 337, 1979-1992) (900 mg, 3.05 mmol) in MeOH (25 mL) and NH4OH (28% aqueous solution, 0.4 mL) was added Raney-Nickel (˜3 g). The mixture was hydrogenated at room temperature under atmosphere pressure for 20 h. The catalyst was filtered off and washed with MeOH. Solvents were evaporated to give the crude product. This was purified by silica gel chromatography, eluted with 15% MeOH in DCM and 83:14:3 DCM-MeOH-ammonia to give pure rac-(2R,4aR,6R,7S,8R,8aR)-7-amino-2-phenylhexahydro-4H-benzo[d][1,3]dioxine-6,8-diol (653 mg, 81%) as a white solid. 1H NMR (600 MHz, CD3OD) δ 7.52-7.50 (m, 2H), 7.37-7.32 (m, 3H), 5.58 (s, 1H), 4.13 (dd, J=11.0, 4.3, 1H), 3.68 (t, J=11.0, 1H), 3.51-3.41 (m, 3H), 2.67 (t, J=9.3, 1H), 1.83-1.76 (m, 2H), 1.17 (q, J=13.0, 1H).

후처리

  1. filtrationThe catalyst was filtered off
  2. washwashed with MeOH
  3. customSolvents were evaporated
  4. customto give the crude product
  5. customThis was purified by silica gel chromatography
  6. washeluted with 15% MeOH in DCM and 83:14:3 DCM-MeOH-ammonia

출처 및 근거

ORD 기록
ord-aefe3208ac784f8cb1375dbb36d45ba6
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09120781B2

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