Dichloromethane → N-(Carbamoylmethyl)-N-(thymin-1-ylacetyl)-beta-alanine ethyl ester

HRID 51185

反応式

HRID 51185 の反応式
[N:1]1([CH2:10][C:11]([OH:13])=O)[CH:9]=[C:7]([CH3:8])[C:5](=[O:6])[NH:4][C:2]1=[O:3].C(Cl)Cl.[CH2:17]([O:19][C:20](=[O:28])[CH2:21][CH2:22][NH:23][CH2:24][C:25](=[O:27])[NH2:26])[CH3:18].C1CCC(N=C=NC2CCCCC2)CC1>CN(C=O)C.CN(C=O)C.C(Cl)Cl>[CH2:17]([O:19][C:20](=[O:28])[CH2:21][CH2:22][N:23]([CH2:24][C:25](=[O:27])[NH2:26])[C:11](=[O:13])[CH2:10][N:1]1[CH:9]=[C:7]([CH3:8])[C:5](=[O:6])[NH:4][C:2]1=[O:3])[CH3:18]

参加物

7

反応条件

温度
0 °C

実験手順

DhbtOH (9.37 g, 57.4 mmol), N1-thyminyl acetic acid (10.57 g, 57.4 mmol) and CH2Cl2 (100 mL) were added to a solution of N-(carbamoylmethyl)-β-alanine ethylester (10.0 g, 57.4 mmol) in dry DMF (100 mL). The solution was cooled to 0° C. in an ice bath and a solution of DCC (1.90 g, 9.18 mmol) in DMF/CH2Cl2 (100 mL, 1:1 v/v) was added dropwise within 20 minutes. The ice bath was removed and after stirring for 1 hour at room temperature. The reaction mixture was filtered and the precipitate (DCU) was rinsed with CH2Cl2 (50 mL). The organic solution and the CH2Cl2 rinse were combined. A colorless precipitate formed overnight which was filtered and rinsed with CH2Cl2. The precipitate was dried in vacuo to give 12.0 g (61%) (mp 207-208° C.) of the title compound.

後処理

  1. customThe ice bath was removed
  2. filtrationThe reaction mixture was filtered
  3. washthe precipitate (DCU) was rinsed with CH2Cl2 (50 mL)
  4. washThe organic solution and the CH2Cl2 rinse
  5. customA colorless precipitate formed overnight which
  6. filtrationwas filtered
  7. washrinsed with CH2Cl2
  8. customThe precipitate was dried in vacuo

出典と根拠

ORDレコード
ord-e79c5c77798049f2af95b4ccefdf6e6b
出典データセット
uspto-grants-2004_03
特許番号
US06713602B1

関連ノート

読み込み中…