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Thiourea → HCID 86685413、化合物

HRID 1911001
ノート
印刷プレビュー

反応式

HRID 1911001 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[CH2:11][CH2:10][CH2:9][C:8]([CH2:12][Cl:13])=[CH:7][C:6]=2[CH:14]=1.[NH2:15][C:16]([NH2:18])=[S:17]>C(O)C>[ClH:13].[C:16]([S:17][CH2:12][C:8]1[CH2:9][CH2:10][CH2:11][C:5]2[CH:4]=[CH:3][C:2]([Br:1])=[CH:14][C:6]=2[CH:7]=1)(=[NH:15])[NH2:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 2723790ThioureaHCID 86685412HCID 86685412、化合物

生成物 1

HCID 86685413HCID 86685413、化合物収率 91%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of 2-bromo-8-(chloromethyl)-6,7-dihydro-5H-benzo[7]annulene from step A6 (60 mg, 0.221 mmol) in ethanol (1 mL) was added thiourea (16.82 mg, 0.221 mmol). The mixture was heated at reflux for 4 h. The solvent was removed, and the solid residue was triturated with hexanes and dried in vacuo to give (2-bromo-6,7-dihydro-5H-benzo[7]annulen-8-yl)methyl carbamimidothioate hydrochloride (70 mg, 0.201 mmol, 91% yield). To a solution of (2-bromo-6,7-dihydro-5H-benzo[7]annulen-8-yl)methyl carbamimidothioate, hydrochloride (60 mg, 0.173 mmol) in TFA (1 mL) was added triflic acid (0.2 mL) at 0° C. The mixture was stirred at rt for 18 h and then heated to 80° C. for 4 h. Another 2 mL of TFA and 0.2 mL of trifilic acid were added, and the mixture was stirred at 60° C. for 20 h. The solvent was removed. The residue was dissolved in 50 mL of EtOAc and the organic layer was washed with saturated sodium bicarbonate/water, dried over sodium sulfate, filtered, and concentrated in vacuo to afford crude product (60 mg, 0.193 mmol, 112% yield), which was used for the next step without purification.

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 4 h
  3. customThe solvent was removed
  4. customthe solid residue was triturated with hexanes
  5. customdried in vacuo

出典と根拠

ORDレコード
ord-15d4e2533faf471eb2e29993b2622d13
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08604024B2

反応ノート

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