Diisopropylethylamine → HCID 58864391, 화합물

HRID 1353503노트

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HRID 1353503 반응식
[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([CH2:17][CH:18]([NH2:23])[C:19]([O:21][CH3:22])=[O:20])=[CH:14][CH:15]=2)[CH:10]=[N:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C1C(=O)N(OC(ON2C(=O)CCC2=O)=O)[C:26](=[O:27])C1.C(N(CC)C(C)C)(C)C.[NH:51]1[CH2:56][CH2:55][CH:54]([N:57]2[CH2:66][C:65]3[C:60](=[CH:61][CH:62]=[CH:63][CH:64]=3)[NH:59][C:58]2=[O:67])[CH2:53][CH2:52]1>C(Cl)Cl>[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([CH2:17][CH:18]([C:19]([O:21][CH3:22])=[O:20])[NH:23][C:26]([N:51]3[CH2:52][CH2:53][CH:54]([N:57]4[CH2:66][C:65]5[C:60](=[CH:61][CH:62]=[CH:63][CH:64]=5)[NH:59][C:58]4=[O:67])[CH2:55][CH2:56]3)=[O:27])=[CH:14][CH:15]=2)[CH:10]=[N:9]1)=[O:7])([CH3:3])([CH3:4])[CH3:2]

참가 물질

6

실험 절차

A solution of 5-(2-amino-2-methoxycarbonyl-ethyl)-indazole-1-carboxylic acid tert-butyl ester (307 mg, 0.96 mmol), N,N-disuccinimidyl carbonate (246 mg, 0.961 mmol), and N,N-diisopropylethylamine (0.67 mL, 3.84 mmol) in methylene chloride was stirred for 30 min at room temperature. 3-piperidin-4-yl-3,4-dihydro-1H-quinazolin-2-one (238 mg, 1.03 mmol) was added and the reaction mixture was stirred at room temperature for 16 h. The solvent was evaporated and the residue subjected to flash chromatography using methylene chloride/methanol/triethylamine (93:5:2) as eluent, giving the product (259 mg, 47%). 1H-NMR (CDCl3, 300 MHz) δ 8.13–8.10 (m, 2H), 7.48 (br s, 1H), 7.31 (dd, J=8.8, 1.6 Hz, 1H), 7.16 (t, J=8.0 Hz, 1H), 7.05 (d, J=7.0 Hz, 1H), 6.94 (t, J=7.7 Hz, 1H), 6.82 (s, 1H), 6.66 (d, J=8.0 Hz, 1H), 4.98 (d, J=7.7 Hz, 1H), 4.87–4.81 (m, 1H), 4.58–4.49 (m, 1H), 4.26 (s, 2H), 4.05–3.97 (m, 2H), 3.74–3.67 (m, 4H), 3.29–3.23 (m, 2H), 2.93–2.84 (m, 2H), 1.76–1.62 (m, 1H), 1.70 (s, 9H), 1.48–1.42 (m, 1H). Mass spec.: 577 (MH)+.

후처리

  1. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-033c9c87312643bebdd6c00b3a5855f4
출처 데이터셋
uspto-grants-2007_05
특허 번호
US07220862B2

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