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Nitrogen → Arq-621

HRID 1517351
ノート
印刷プレビュー

反応式

HRID 1517351 の反応式
[Cl:1][C:2]1[C:3]([F:48])=[C:4]([CH:45]=[CH:46][CH:47]=1)[C:5]([N:7]([C@@H:22]([C:26]1[N:35]([NH:36][C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[C:34](=[O:43])[C:33]2[C:28](=[CH:29][C:30]([Cl:44])=[CH:31][CH:32]=2)[N:27]=1)[CH2:23][C:24]#[CH:25])[CH2:8][CH2:9][CH2:10][N:11]1C(=O)C2C(=CC=CC=2)C1=O)=[O:6].N#N.NN>CO>[NH2:11][CH2:10][CH2:9][CH2:8][N:7]([C@@H:22]([C:26]1[N:35]([NH:36][C:37]2[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=2)[C:34](=[O:43])[C:33]2[C:28](=[CH:29][C:30]([Cl:44])=[CH:31][CH:32]=2)[N:27]=1)[CH2:23][C:24]#[CH:25])[C:5](=[O:6])[C:4]1[CH:45]=[CH:46][CH:47]=[C:2]([Cl:1])[C:3]=1[F:48]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 947NitrogenHCID 9321HydrazineHCID 576954593-chloro-N-[(R)-1-(7-chloro-4-oxo-3-phenylamino-3,4-dihydro-quinazolin-2-yl)-but-3-ynyl]-N-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)propyl]-2-fluoro-benzamide

生成物 1

HCID 25110841Arq-621収率 91%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of (R)-3-chloro-N-[1-(7-chloro-4-oxo-3-phenylamino-3,4-dihydro-quinazolin-2-yl)-but-3-ynyl]-N-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-2-fluoro-benzamide (1.13 g, 1.65 mmol) in methanol (10 ml) and the solution was purged with N2. To this solution was added hydrazine (110 μl). The mixture was then stirred at room temperature and the reaction progress was monitored by HPLC/MS. The reaction mixture was then filtered and solvent was removed from the filtrate. The residue was purified by flash column to afford N-(3-amino-propyl)-3-chloro-N-[(R)-1-(7-chloro-4-oxo-3-phenylamino-3,4-dihydro-quinazolin-2-yl)-but-3-ynyl]-2-fluoro-benzamide (708 mg, 91%) as off-white solid, M.p. 101-103° C. LCMS: m/e 552 [M+H]. 1H NMR (CDCl3): δ 8.13 (d, J=8.8 Hz, 1H), 7.83 (s, 1H), 7.45 (dd, J=4.8 and 2.0 Hz, 1H), 7.32 (m, 1H), 7.22 (t, J=8.0 Hz, 1H), 7.15 (t, J=8.0 Hz, 1H), 7.05 (t, J=8.0 Hz, 1H), 6.95 (m, 1H), 6.84 (t, J=7.2 Hz, 1H), 6.72 (d, J=7.2 Hz, 1H), 6.48 (d, J=7.2 Hz 1H), 3.62 (m, 1H), 3.48 (m, 1H), 3.28 (br, 1H), 3.14 (m, 1H), 3.02 (br, 1H), 2.59 (m, 2H), 2.30 (br, 1H), 2.02 (t, 2.4 Hz, 1H), 1.36 (m, 2H).

後処理

  1. filtrationThe reaction mixture was then filtered
  2. customsolvent was removed from the filtrate
  3. customThe residue was purified by flash column

出典と根拠

ORDレコード
ord-51d7d0a390044e909766ada919e7e8d7
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08232285B2

反応ノート

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