Ethylamine → HCID 21094177, compound

HRID 729707Notes

Reaction equation

HRID 729707 reaction equation
Cl[S:2]([C:5]1[CH:10]=[CH:9][C:8]([CH:11]([CH2:17][CH:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)[C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:7][CH:6]=1)(=[O:4])=[O:3].S(Cl)(Cl)(=O)=O.[CH2:29]([NH2:31])[CH3:30]>C1COCC1>[CH2:29]([NH:31][S:2]([C:5]1[CH:10]=[CH:9][C:8]([CH:11]([CH2:17][CH:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)[C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:7][CH:6]=1)(=[O:4])=[O:3])[CH3:30]

Participants

5

Reactant 3

HCID 6341EthylamineHCID 24648Sulfuryl chlorideHCID 21094170HCID 21094170, compound

Product 1

HCID 21094177HCID 21094177, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
20 °C

Procedure

Ethyl(4-nitrophenyl)acetate (25.0 g, 119.5 mmol) was alkylated with 4-iodomethyltetrahydropyran (32.4 g, 143.4 mmol), according to the protocol described in Preparation 41, to give ethyl 2-(4-nitrophenyl)-3-(tetrahydropyran-4-yl)propionate: δH (CDCl3): 1.21 (3H, t), 1.25-1.45 (3H, m), 1.55-1.65 (2H, m), 1.70-1.80 (1H, m), 2.05-2.15 (1H, m), 3.25-3.35 (2H, m), 3.79 (1H, t), 3.90-3.95 (2H, m), 4.10-4.20 (2H, m), 7.49 (2H, d), 8.19 (2H, d). The nitro group of this compound (6.55 g, 18.1 mmol) was reduced utilising the procedure described in EXAMPLE 145 to give ethyl 2-(4-aminophenyl)-3-(tetrahydropyran-4-yl)propionate: m/z (ES+)=278.2 [M+H]+. This compound (30.5 g, 110 mmol) was transformed into ethyl 2-(4-chlorosulfonylphenyl)-3-(tetrahydropyran-4-yl)propionate employing the protocol described in Preparation 59. A solution of this sulfonyl chloride (33.6 g, 93.2 mmol) in anhydrous THF (100 mL) was added over 30 min at 0° C. to EtNH2 (116.5 mL of a 2.0M solution in THF, 233.0 mmol). The mixture was warmed up to 20° C., before being stirred for 16 h. The suspension was filtered through a Celite pad, which was washed with THF (3×50 mL). The combined THF solutions were concentrated to furnish crude ethyl 2-(4-ethylsulfamoylphenyl)-3-(tetrahydropyran-4-yl)propionate: m/z (ES+)=370.2 [M+H]+. Hydrolysis of this ester (33.7 g, 91.2 mmol), utilising the procedure outlined in Preparation 41, followed by purification via RP-HPLC afforded the title compound: m/z (ES+)=342.2 [M+H]+.

Workup

  1. customdescribed in Preparation 59
  2. filtrationThe suspension was filtered through a Celite pad, which
  3. washwas washed with THF (3×50 mL)
  4. concentrationThe combined THF solutions were concentrated

Sources & evidence

ORD record
ord-8161ef5558be4d1d9a94ab3737eb0f26
Source dataset
uspto-grants-2009_09
Patent number
US07582632B2

Reaction notes

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