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Allyl bromide → HCID 131726277、化合物

HRID 351189
ノート
印刷プレビュー

反応式

HRID 351189 の反応式
P(Br)(Br)[Br:2].C1CCC(C2(CN3N=CN=C3)CCN(C([C@H](NC([C@@H:31]3[NH:40][CH2:39][C:38]4[C:33](=[CH:34][CH:35]=[CH:36][CH:37]=4)[CH2:32]3)=O)CC3C=CC(Cl)=CC=3)=O)CC2)CC1.[CH2:47](Br)[CH:48]=[CH2:49].CCN(C(C)C)C(C)C>C(Cl)Cl.CN(C=O)C>[BrH:2].[CH2:49]([N:40]1[CH2:31][CH2:32][CH:33]2[C:38](=[CH:37][CH:36]=[CH:35][CH2:34]2)[CH2:39]1)[CH:48]=[CH2:47]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 7841Allyl bromideHCID 24614Phosphorus tribromideHCID 81531DiisopropylethylamineHCID 9938402(3R)-N-((1R)-1-((4-Chlorophenyl)methyl)-2-(4-cyclohexyl-4-(1H-1,2,4-triazol-1-ylmethyl)-1-piperidinyl)-2-oxoethyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxamide

生成物 1

HCID 131726277HCID 131726277、化合物収率 59%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒
HCID 6344Dichloromethane溶媒2 回

実験手順

resin 2 (0.65 mmol g−1 (est.), 1.49 g) in dry DCM (25 cm3) were treated with PBr3 (2.28 mmol, 216 mm3) at 20° C. for 12 h. The resin was filtered off, washed with DCM (200 cm3), dried at air and transferred to a flask with DMF (20 cm3) and THIQ (5.7 mmol, 725 mm3) was added. The resin was stirred at r.t. for 24 h, washed with DMF, MeOH, DCM, and MeOH. It was dried under high vacuum. 1.45 g (0.5 mmol g−1 (est.)) of it was resuspended in DMF (10 cm3) and allyl bromide (150 mm3, 1.7 mmol) was added. After 5 d at 20° C. the solid was filtered off, washed with DMF (100 cm3) and DCM (100 cm3). The resin was then treated with DIPEA (1.00 mmol, 175 mm3) in DCM (25 cm3). After 2 days the solid material was filtered off and washed with DCM and MeOH. Yield of resin 3 1.28 g (max. est. yield: 1.25 g). The solvent was removed from the filtrate and gave analytical pure 4 (0.47 mmol, 120 mg, 59%) as a white solid.

後処理

  1. filtrationThe resin was filtered off
  2. washwashed with DCM (200 cm3)
  3. customdried at air
  4. additionwas added
  5. washwashed with DMF, MeOH, DCM, and MeOH
  6. customIt was dried under high vacuum
  7. filtrationAfter 5 d at 20° C. the solid was filtered off
  8. washwashed with DMF (100 cm3) and DCM (100 cm3)
  9. filtrationAfter 2 days the solid material was filtered off
  10. washwashed with DCM and MeOH
  11. customThe solvent was removed from the filtrate

出典と根拠

ORDレコード
ord-9509a590137e498dae6fd5594241a132
出典データセット
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07183367B2

反応ノート

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