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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 1-{4-[7,8-Dimethyl-6-(methylsulfanyl)-3-phenylimidazo[1,2-b]pyridazin-2-yl]-phenyl}cyclobutanamine

HRID 1501364
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HRID 1501364 반응식
[CH3:1][C:2]1[C:7]([S:8][CH3:9])=[N:6][N:5]2[C:10]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=3)=[C:11]([C:13]3[CH:18]=[CH:17][C:16]([C:19]4([NH:23]C(=O)OC(C)(C)C)[CH2:22][CH2:21][CH2:20]4)=[CH:15][CH:14]=3)[N:12]=[C:4]2[C:3]=1[CH3:37].CO.Cl.O1CCOCC1>C(Cl)Cl>[CH3:1][C:2]1[C:7]([S:8][CH3:9])=[N:6][N:5]2[C:10]([C:31]3[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=3)=[C:11]([C:13]3[CH:14]=[CH:15][C:16]([C:19]4([NH2:23])[CH2:22][CH2:21][CH2:20]4)=[CH:17][CH:18]=3)[N:12]=[C:4]2[C:3]=1[CH3:37]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 312751,4-DioxaneHCID 70856623HCID 70856623, 화합물

생성물 1

HCID 708179531-{4-[7,8-Dimethyl-6-(methylsulfanyl)-3-phenylimidazo[1,2-b]pyridazin-2-yl]-phenyl}cyclobutanamine수율 94%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매
2회

실험 절차

To a mixture of the tert-butyl (1-{4-[7,8-dimethyl-6-(methylsulfanyl)-3-phenylimidazo[1,2-b]pyridazin-2-yl]phenyl}cyclobutyl)carbamate that was prepared in a manner analgous to that described for Intermediate Example Int-35 (95 mg, 0.190 mmol, 1.0 eq) in DCM (1.19 mL) and MeOH (0.75 mL) was added a solution of 4 M hydrogen chloride in dioxane (0.92 mL, 3.69 mmol, 20.0 eq) and the mixture was stirred overnight at rt. The mixture was poured onto ice, made alkaline, treated with DCM and filtered through a phase separator. The volatile components of the organic phase were removed in vacuo to give 75 mg (94% yield) of the title compound.

후처리

  1. customwas prepared in a manner analgous to
  2. additionThe mixture was poured onto ice
  3. filtrationfiltered through a phase separator
  4. customThe volatile components of the organic phase were removed in vacuo

출처 및 근거

ORD 기록
ord-5aa3c7cfbc1644f7bd64904d81a2dd5d
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09206185B2

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