Diisopropylamine → 9-Methylene-9H-fluorene

HRID 842410

反応式

HRID 842410 の反応式
CC1C=CC(C(N)C2C=CC=CC=2)=CC=1.[CH:16]1[C:28]2[CH:27]([CH2:29]OC(N[C@H](C(NC(B3OC(CCC(C)CC(O)=O)(C)C(C)(C)O3)CC)=O)CC(C)C)=O)[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[C:20]=2[CH:19]=[CH:18][CH:17]=1.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2C=CC=CC=2N=N1.C(NC(C)C)(C)C.C(OC(=O)C)(=O)C.CN1CCOCC1>CN(C)C=O>[CH2:29]=[C:27]1[C:28]2[C:20](=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:21]2[C:26]1=[CH:25][CH:24]=[CH:23][CH:22]=2

参加物

8

実験手順

5 g (5.25 mmol) of 4-methylbenzhydrylamine resin were swollen in dimethylformamide and excess solvent was drained from the resin. The resin was then resuspended in dimethylformamide containing 3.4 g (5.48 mmol) of 5-[2-[1(RS)-[[N-[(9-fluorenyl)methoxycarbonyl]-L-leucyl]amino]propyl]-4(RS),5,5-trimethyl-1,3,2-dioxaborolan-4-yl]-3(RS)-methylvaleric acid and 3 g (8.2 mmol) of 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate. Thereto were added 3.0 ml (16.5 mmol) of diisopropylamine. The resulting mixture was agitated for 100 minutes and the resin was then drained and washed three times with dimethylformamide. The resin was then resuspended in dimethylformamide containing 5 ml (54.8 mmol) of acetic anhydride and 11.5 ml (110 mmol) of N-methylmorpholine. The mixture was agitated for 30 minutes and the resin was then drained. The resin was then resuspended in dimethylformamide containing 5 ml (54.8 mmol) of acetic anhydride and 11.5 ml (110 mmol) of N-methylmorpholine. The mixture was agitated for 30 minutes and the resin was then drained and washed three times with dimethylformamide, twice with ethyl acetate, twice with dichloromethane and twice with diethyl ether and then dried under a vacuum. After drying there was obtained 6 g of 5-[2-[1(RS)-[[N-[(9-fluorenyl)methoxycarbonyl]-L-leucyl]amino]propyl]-4-(RS),5,5-trimethyl-1,3 ,2-dioxoborolan-4-yl]-3(RS)-methyl-N-(RS)-(4-methylphenyl)-benzyl]valeramide-polystyrene conjugate as a pale brown solid (0.25 mmol/g loading estimated by quantitation of dibenzofulvene at 301 nM).

後処理

  1. washwashed three times with dimethylformamide
  2. stirringThe mixture was agitated for 30 minutes
  3. stirringThe mixture was agitated for 30 minutes
  4. washwashed three times with dimethylformamide
  5. dry with materialtwice with ethyl acetate, twice with dichloromethane and twice with diethyl ether and then dried under a vacuum
  6. customAfter drying there

出典と根拠

ORDレコード
ord-3b50589ce1024e90b7afad10eaf0d5d5
出典データセット
uspto-grants-2002_04
特許番号
US06372883B1

関連ノート

読み込み中…