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1,1'-Carbonyldiimidazole → N-(1-(5-carbamoylpyridin-2-yl)piperidin-4-yl)-4-isopropylpiperazine-1-carboxamide

HRID 1504599
ノート
印刷プレビュー

反応式

HRID 1504599 の反応式
Cl.[NH2:2][CH:3]1[CH2:8][CH2:7][N:6]([C:9]2[CH:17]=[CH:16][C:12]([C:13]([NH2:15])=[O:14])=[CH:11][N:10]=2)[CH2:5][CH2:4]1.[CH3:18][CH2:19][N:20]([CH:24]([CH3:26])[CH3:25])[CH:21](C)[CH3:22].[C:27](N1C=CN=C1)([N:29]1C=CN=C1)=[O:28].C(N1CCNCC1)(C)C>CN(C=O)C>[C:13]([C:12]1[CH:16]=[CH:17][C:9]([N:6]2[CH2:5][CH2:4][CH:3]([NH:2][C:27]([N:29]3[CH2:22][CH2:21][N:20]([CH:24]([CH3:26])[CH3:25])[CH2:19][CH2:18]3)=[O:28])[CH2:8][CH2:7]2)=[N:10][CH:11]=1)(=[O:14])[NH2:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 682631,1'-CarbonyldiimidazoleHCID 780131-IsopropylpiperazineHCID 81531DiisopropylethylamineHCID 693590386-(4-Aminopiperidin-1-yl)nicotinamide hydrochloride

生成物 1

HCID 86730057N-(1-(5-carbamoylpyridin-2-yl)piperidin-4-yl)-4-isopropylpiperazine-1-carboxamide収率 8%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

To a cooled solution (0-5° C.) of 6-(4-aminopiperidin-1-yl)nicotinamide hydrochloride (293 mg, 1 mmol) in 5 ml DMF was added DIPEA (645 mg, 2.2 mmol) and 1,1′-carbonyldiimidazole (170 mg, 1.05 mmol). After stirring for 1 h, 1-isopropylpiperazine (154 mg, 1.2 mmol) was added and the resulting mixture was warmed to room temperature for 16 h. The crude mixture was filtered through Celite and the filtrate was purified by preparative HPLC to give title compound (30 mg, 8%) as an off-white solid. [1HNMR (400 MHz, DMSO-d6) δ 8.60 (d, 1H), 7.94 (m, 1H), 7.73 (s, 1H), 7.10 (s, 1H), 6.86 (d, 1H), 6.21 (d, 1H), 4.37 (d, 2H), 3.65 (m, 1H), 3.23 (t, 4H), 2.94 (t, 2H) 2.62 (m, 1H), 2.34 (t, 4H), 1.78 (d, 2H), 1.36 (m, 2H), 0.96 (d, 6H); LCMS RtB=1.53 min, [M+H]+=375.2].

後処理

  1. filtrationThe crude mixture was filtered through Celite
  2. customthe filtrate was purified by preparative HPLC

出典と根拠

ORDレコード
ord-d6668632bbc64f18b9250b2827ba5cc7
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09216182B2

反応ノート

読み込み中…

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