Dimethylformamide → HCID 178501117, compound
Reaction equation
ClS([N:5]=C=O)(=O)=O.[CH3:8][O:9][C:10]([C@H:12]1[CH2:17][CH2:16][C@H:15]([C:18](O)=O)[CH2:14][CH2:13]1)=[O:11].CN(C)C=O>C(Cl)Cl>[C:18]([C@H:15]1[CH2:16][CH2:17][C@H:12]([C:10]([O:9][CH3:8])=[O:11])[CH2:13][CH2:14]1)#[N:5]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
Chlorosulfonyl isocyanate (1.0 mL, 0.012 mol) was added to a solution of trans-4-(methoxycarbonyl)cyclohexanecarboxylic acid (2.00 g, 0.0107 mol) in DCM cooled to 0° C. The resulting solution was heated at reflux for 15 minutes and then cooled 0° C. and treated dropwise with DMF. The mixture was stirred at room temperature overnight then poured onto ice water and the organic phase separated and washed with a saturated solution of sodium bicarbonate. The solvent was removed in vacuo and the crude material was taken up in ethyl acetate, washed with 1N aq. NaOH (10 mL) and the ethyl acetate removed in vacuo. The resulting crude product was used in subsequent steps without further purification. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.36-1.70 (4H, m), 2.01-2.18 (4H, m), 2.24-2.54 (2H, m) and 3.68 (3H, s).
Workup
- temperatureThe resulting solution was heated
- temperatureat reflux for 15 minutes
- temperaturecooled 0° C.
- additionthen poured onto ice water
- customthe organic phase separated
- washwashed with a saturated solution of sodium bicarbonate
- customThe solvent was removed in vacuo
- washwashed with 1N aq. NaOH (10 mL)
- customthe ethyl acetate removed in vacuo
- customThe resulting crude product was used in subsequent steps without further purification
Sources & evidence
- ORD record
- ord-df40b7d47a734d05914e4c9b62d17d8b
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08796455B2
Reaction notes
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