4-Nitrobenzyl chloroformate → HCID 18677664, compound
Reaction equation
[CH2:1]([NH:4][CH:5]1[CH2:10][CH2:9][N:8]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:7][CH2:6]1)[CH:2]=[CH2:3].C(N(CC)C(C)C)(C)C.Cl[C:28]([O:30][CH2:31][C:32]1[CH:37]=[CH:36][C:35]([N+:38]([O-:40])=[O:39])=[CH:34][CH:33]=1)=[O:29]>ClCCl.C(OCC)(=O)C>[C:14]([O:13][C:11]([N:8]1[CH2:7][CH2:6][CH:5]([N:4]([C:28]([O:30][CH2:31][C:32]2[CH:33]=[CH:34][C:35]([N+:38]([O-:40])=[O:39])=[CH:36][CH:37]=2)=[O:29])[CH2:1][CH:2]=[CH2:3])[CH2:10][CH2:9]1)=[O:12])([CH3:17])([CH3:16])[CH3:15]Participants
6
Procedure
A portion of the crude 4-(allylamino)-1-(tert-butoxycarbonyl)piperidine (400 mg, 1.66 mmol) was dissolved in 10 mL of dichloromethane and treated with N,N-diisopropylethylamine (0.700 mL, 519 mg, 4.0 mmol) and 4-nitrobenzyl chloroformate (392 mg, 1.82 mmol). After stirring 3 h at rt, the mixture was diluted with 30 mL of ethyl acetate and washed with 15 mL each of 2 N aqueous HCl, saturated aqueous sodium bicarbonate, and brine. The organic layer was dried over sodium sulfate, and evaporated. The residue was purified by FC on silica gel, eluting with 30% ethyl acetate in hexane, to give 572 mg of the title compound as a colorless syrup.
Workup
- washwashed with 15 mL each of 2 N aqueous HCl, saturated aqueous sodium bicarbonate, and brine
- dry with materialThe organic layer was dried over sodium sulfate
- customevaporated
- customThe residue was purified by FC on silica gel
- washeluting with 30% ethyl acetate in hexane
Sources & evidence
- ORD record
- ord-a1ededd305de4a40a13def76090bd285
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506777B1
Reaction notes
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