tert-Butyl 4-(bromomethyl)-1H-benzo[d]imidazole-1-carboxylate → 5,6-Dihydro-N,N-dimethyl-4H-pyrrolo(3,2,1ij)quinolin-5-amine

HRID 327478

反応式

Br[CH2:2][C:3]1[C:11]2[N:10]=[CH:9]N(C(OC(C)(C)C)=O)[C:7]=2[CH:6]=[CH:5][CH:4]=1.[CH2:19]([N:22]([CH:26]([C:32](OCC)=O)[C:27](OCC)=O)[CH2:23]CC)CC>C1COCC1.CCOCC>[CH3:19][N:22]([CH3:23])[CH:26]1[CH2:32][C:7]2[C:11]3=[C:3]([CH:2]=[CH:9][N:10]3[CH2:27]1)[CH:4]=[CH:5][CH:6]=2

参加物

実験手順

This compound was prepared by following the procedure of Example 18, but substituting methyl 7-(bromomethyl)-1H-indole-1-carboxylate for t-butyl 4-(bromomethyl)-1H-benzimidazole-1-carboxylate and diethyl (dimethylamino)malonte for diethyl (dipropylamino)malonate. The bulk of the product was converted to the maleate salt, mp 114°-115° C. from THF/ether.

後処理

customThis compound was prepared

出典と根拠

ORDレコード: ord-556cf091629349e592814e7e8c44d29f
出典データセット: uspto-grants-1993_12
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US05273975

反応式

参加物

反応物 2

生成物 1

試薬・触媒・溶媒 1

実験手順

後処理

出典と根拠

関連ノート