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Hydrochloric Acid → 2-(4-chloro-3,5-diphenyl-1H-pyrazolo[3,4-c]pyridazin-1-yl)acetic acid

HRID 1775550
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HRID 1775550 반응식
[NH2:1][C:2]1[N:6]([CH2:7][C:8]([O-:10])=[O:9])[N:5]=[C:4]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:3]=1[C:17]#[C:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[Na+].[N:26]([O-])=O.[Na+].[ClH:30]>C(OCC)C.O>[Cl:30][C:17]1[C:18]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[N:26][N:1]=[C:2]2[N:6]([CH2:7][C:8]([OH:10])=[O:9])[N:5]=[C:4]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:3]=12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 23668193Sodium NitriteHCID 70982572sodium 2-(5-amino-3-phenyl-4-(phenylethynyl)-1H-pyrazol-1-yl)acetate

생성물 1

HCID 665757822-(4-chloro-3,5-diphenyl-1H-pyrazolo[3,4-c]pyridazin-1-yl)acetic acid

시약·촉매·용매 2

HCID 962Water용매HCID 3283
Diethyl Ether
용매

실험 절차

A suspension of sodium 2-(5-amino-3-phenyl-4-(phenylethynyl)-1H-pyrazol-1-yl)acetate (2 g, 6.0 mmol) in diethylether (10 mL) and concentrated HCl (50 mL) was cooled at −15° C. before sodium nitrite (0.62 g, 8.0 mmol) in water (5 mL) was added dropwise. The solution was allowed to warm up to room temperature and left stirring for further 18 h. The reaction mixture was carefully quenched with an aqueous solution of Na2CO3 at 10° C., until pH basic, and then extracted EtOAc, backwashed with water then brine, dried (MgSO4) and concentrated in vacuo. The resultant residue was purified using chromatography (silica gel, gradient 2 to 10% diethylether/CH2Cl2) yielding Compound 47 as a yellow foam (580 mg).

후처리

  1. additionwas added dropwise
  2. waitleft
  3. customThe reaction mixture was carefully quenched with an aqueous solution of Na2CO3 at 10° C.
  4. dry with materialbrine, dried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customThe resultant residue was purified

출처 및 근거

ORD 기록
ord-91d5e2090b5843c382407a9dd8e28efe
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09260381B2

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