Sodium hydride → HCID 178459818, compound
Reaction equation
[CH2:1]([O:4][C:5]([NH:7][C:8]1([C:11]2[CH:19]=[CH:18][C:14]([C:15]([OH:17])=O)=[CH:13][CH:12]=2)[CH2:10][CH2:9]1)=[O:6])[CH:2]=[CH2:3].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[O:42]1[C:50]2[C:45](=[CH:46][CH:47]=[CH:48][CH:49]=2)[CH2:44][C:43]1=[O:51].[H-].[Na+]>CN(C=O)C.O.C(O)(=O)C.C(N(CC)CC)C>[CH2:1]([O:4][C:5](=[O:6])[NH:7][C:8]1([C:11]2[CH:12]=[CH:13][C:14]([C:15]([OH:17])=[C:44]3[C:45]4[CH:46]=[CH:47][CH:48]=[CH:49][C:50]=4[O:42][C:43]3=[O:51])=[CH:18][CH:19]=2)[CH2:9][CH2:10]1)[CH:2]=[CH2:3]Participants
9
Reactant 4
Product 1
Reagents, catalysts & solvents 4
Procedure
0.8 g of 4-(1-allyloxycarbonylaminocyclopropyl)benzoic acid and 0.585 mL of triethylamine were dissolved in 10 mL of anhydrous DMF and combined with 1.16 g of TBTU, stirred for 15 minutes at RT, then combined with 0.4 g of coumaranone and stirred for a further 10 minutes. While cooling with the ice bath, 0.42 g of NaH was added batchwise as a 60% suspension in white oil, the mixture was stirred for 2 hours at RT and, once the reaction had ended, the mixture was diluted with water to a total volume of approximately 150 mL. The mixture was acidified with 2N acetic acid. The crystals were suction filtered and washed with water. Yield: 1.1 g of solid with a melting point of 125° C.-126° C.
Workup
- stirringstirred for a further 10 minutes
- stirringthe mixture was stirred for 2 hours at RT
- filtrationfiltered
- washwashed with water
Sources & evidence
- ORD record
- ord-0a191095267349c2abd8e12ddddcdaca
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07723381B2
Reaction notes
Loading…