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Hydrochloric Acid → 2-[3-(4-Cyanobenzyl)-3h-imidazol-1-yl]-n-benzyl-n-(1-phenylpiperidin-4-yl)acetamide hydrochloride

HRID 443310
ノート
印刷プレビュー

反応式

HRID 443310 の反応式
[CH2:1]([NH:8][CH:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:11][CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:21]([C:23]1[CH:38]=[CH:37][C:26]([CH2:27][N:28]2[C:32](CC([O-])=O)=[CH:31][N:30]=[CH:29]2)=[CH:25][CH:24]=1)#[N:22].[Li+].[OH2:40].ON1C2C=CC=[CH:50][C:45]=2N=N1.[ClH:51].CN(C)CCCN=C=NCC.C(N(CC)C(C)C)(C)C.Cl>C(#N)C>[ClH:51].[C:21]([C:23]1[CH:24]=[CH:25][C:26]([CH2:27][N:28]2[CH:32]=[CH:31][N:30]([CH2:45][C:50]([N:8]([CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[CH:9]3[CH2:14][CH2:13][N:12]([C:15]4[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=4)[CH2:11][CH2:10]3)=[O:40])[CH2:29]2)=[CH:37][CH:38]=1)#[N:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 6

HCID 313Hydrochloric AcidHCID 81531DiisopropylethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 211933851-Phenyl-N'-phenylmethyl-4-piperidinamineHCID 67586058HCID 67586058、化合物

生成物 1

HCID 21193362
2-[3-(4-Cyanobenzyl)-3h-imidazol-1-yl]-n-benzyl-n-(1-phenylpiperidin-4-yl)acetamide hydrochloride

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

Benzyl(1-phenylpiperidin-4-yl)amine (50 mg, 0.188 mmol), lithium [3-(4-cyanobenzyl)-3H-imidazol-4-yl]acetate (51 mg, 0.206 mmol), 1-hydroxybenzotriazole hydrate (38 mg, 0.28 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (72 mg, 0.38 mmol), and N,N-diisopropylethylamine (82 μL, 0.47 mmol) were added to degassed DMF (2 mL) and the mixture was stirred for 18 hrs at room temperature then concentrated in vacuo. The residue was added to sat. NaHCO3 (aq) (5 mL) and extracted with dichloromethane (3×3 mL). The combined organic extracts were dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was chromatographed on silica gel, eluting with dichloromethane--4% methanol--0.01% NH4OH to give the product as a free base. This was lyophilized from HCl (aq)--acetonitrile to give the title compound as a white solid.

後処理

  1. customto degassed DMF (2 mL)
  2. concentrationthen concentrated in vacuo
  3. additionThe residue was added to sat. NaHCO3 (aq) (5 mL)
  4. extractionextracted with dichloromethane (3×3 mL)
  5. dry with materialThe combined organic extracts were dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was chromatographed on silica gel
  9. washeluting with dichloromethane--4% methanol--0.01% NH4OH
  10. customto give the product as a free base

出典と根拠

ORDレコード
ord-755a7783a5254f94944264efb6927491
出典データセット
uspto-grants-1999_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05891889

反応ノート

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