Diethylamine → HCID 59305817, compound
Reaction equation
C1C2C(COC(=O)[NH:17][CH:18]3[CH2:23][CH2:22][CH:21]([C:24]4[N:25]=[C:26]([CH3:29])[S:27][CH:28]=4)[CH2:20][CH2:19]3)C3C(=CC=CC=3)C=2C=CC=1.C(NCC)C>C1COCC1>[CH3:29][C:26]1[S:27][CH:28]=[C:24]([CH:21]2[CH2:22][CH2:23][CH:18]([NH2:17])[CH2:19][CH2:20]2)[N:25]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.10 g (2 mmol) of 9H-fluoren-9-ylmethyl[4-(2-methylthiazol-4-yl)cyclohexyl]carbamate (cis compound) and 15 mL of diethylamine are stirred in 30 mL of THF for 16 hours at ambient temperature. Then the reaction mixture is concentrated by evaporation and the residue is combined with THF and concentrated again by evaporation. The residue is purified by chromatography. Yield: 0.13 g (36%).
Workup
- concentrationThen the reaction mixture is concentrated by evaporation
- concentrationconcentrated again by evaporation
- customThe residue is purified by chromatography
Sources & evidence
- ORD record
- ord-c726c598aa044a9db0ae54c40fa8732c
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07723381B2
Reaction notes
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