ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Acetic Anhydride → HCID 11611808、化合物

HRID 646922
ノート
印刷プレビュー

反応式

HRID 646922 の反応式
F[C:2](F)(F)[C:3](O)=[O:4].[CH3:8][CH:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:20]=[C:19]([N:21]3[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]3)[CH:18]=[CH:17][C:16]=2[NH:27][C:28]([C:30]2[NH:31][CH:32]=[C:33]([C:35]#[N:36])[CH:34]=2)=[O:29])[CH2:11][CH2:10]1.C(OC(=O)C)(=O)C.CCN(C(C)C)C(C)C.C(=O)(O)[O-].[Na+]>ClCCl>[C:3]([N:24]1[CH2:23][CH2:22][N:21]([C:19]2[CH:18]=[CH:17][C:16]([NH:27][C:28]([C:30]3[NH:31][CH:32]=[C:33]([C:35]#[N:36])[CH:34]=3)=[O:29])=[C:15]([N:12]3[CH2:13][CH2:14][CH:9]([CH3:8])[CH2:10][CH2:11]3)[CH:20]=2)[CH2:26][CH2:25]1)(=[O:4])[CH3:2]
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 7918Acetic AnhydrideHCID 81531DiisopropylethylamineHCID 516892Sodium BicarbonateHCID 86604896HCID 86604896、化合物

生成物 1

HCID 11611808HCID 11611808、化合物収率 23.5%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To 4-cyano-1H-pyrrole-2-carboxylic acid [2-(4-methyl-piperidin-1-yl)-4-piperazin-1-yl-phenyl]-amide trifluoroacetic acid salt (as prepared in Example 56, step (b)) (30 mg, 0.048 mmol) in dichloromethane (5 mL) was added acetic anhydride (7.0 μL, 0.072 mmol) and DIEA (31 μL, 0.18 mmol) and the mixture was stirred for 5 h at RT. The mixture was poured into saturated aq sodium bicarbonate (5 mL), extracted with dichloromethane (5 mL), and the organic layer was dried (Na2SO4). The solvents were removed in vacuo and the resulting residue was purified by silica gel preparative TLC eluting with 10% methanol in dichloromethane to yield 4.9 mg (23%) of the title compound as an off-white solid. 1H-NMR (400 MHz, CDCl3): δ 10.57 (br s, 1H), 8.99 (s, 1H), 8.27 (d, 1H, J=8.8 Hz), 7.45 (dd, 1H, J=3.1, 1.3 Hz), 6.851 (s, 1H), 6.81 (d, 1H, J=3.5 Hz), 6.73 (dd, 1H, J=8.9, 2.6 Hz), 3.79 (m, 2H), 3.64 (m, 2H), 3.17-2.96 (m, 4H), 2.74 (m, 2H), 2.70 (m, 2H), 2.15 (s, 3H), 1.87-1.84 (m, 2H), 1.58 (m, 1H), 1.44-1.34 (m, 2H), 1.08 (d, 3H, J=6.5 Hz). LC-MS (ESI, m/z): Calcd. for C24H31N6O2, 435.2 (M+H); found: 435.1.

後処理

  1. extractionextracted with dichloromethane (5 mL)
  2. dry with materialthe organic layer was dried (Na2SO4)
  3. customThe solvents were removed in vacuo
  4. customthe resulting residue was purified by silica gel preparative TLC
  5. washeluting with 10% methanol in dichloromethane

出典と根拠

ORDレコード
ord-eb4b81a0bd66440f80891da76c064a40
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07705042B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート