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Sodium Methoxide → HCID 178473901, 화합물

HRID 1353836
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HRID 1353836 반응식
Cl.C(O[CH:5]([C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[NH:12][N:11]=[C:10]2[C:16]1[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=1)[NH2:6])C.[C:23]([N:26]1[CH2:31][CH2:30][N:29]([CH2:32][C:33]([NH:35][NH2:36])=O)[CH2:28][CH2:27]1)(=[O:25])[CH3:24].C[O-].[Na+]>CO>[C:23]([N:26]1[CH2:31][CH2:30][N:29]([CH2:32][C:33]2[NH:6][C:5]([C:7]3[CH:8]=[C:9]4[C:13](=[CH:14][CH:15]=3)[NH:12][N:11]=[C:10]4[C:16]3[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=3)=[N:36][N:35]=2)[CH2:28][CH2:27]1)(=[O:25])[CH3:24]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

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HCID 10942334Sodium MethoxideHCID 21101187ethoxy[3-(4-fluorophenyl)(1H-indazol-5-yl)]methaneamine hydrochlorideHCID 224797542-(4-acetylpiperazinyl)-N-aminoacetamide

생성물 1

HCID 178473901HCID 178473901, 화합물수율 5.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

The procedure described for Example 283 B was followed using ethoxy[3-(4-fluorophenyl)(1H-indazole-5-yl)]methaneamine hydrochloride (600 mg, 1.88 mmol), 2-(4-acetylpiperazinyl)-N-aminoacetamide (1.12 g, 5.64 mmol), sodium methoxide (1.3 mL, 5.64 mmol), and methanol (8 mL) to yield the title compound (41 mg, 5% yield). 1H NMR (DMSO-d6) δ 13.8 (s, 1H), 8.6 (s, 1H), 8.0 (m, 5H), 7.6 (m, 2H), 7.4 (t, 3H), 4.6 (m, 2H), ES-MS (m/z) 420 [M+1]+.

출처 및 근거

ORD 기록
ord-06f21cdde6f94449bcc778526418650f
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07220771B2

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