1,2-Dichloroethane → HCID 57888765, compound

HRID 1820238Notes

Reaction equation

HRID 1820238 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([NH2:16])[CH2:13][CH2:12][NH:11][CH2:10][C:9]2([CH3:15])[CH3:14])=[CH:4][CH:3]=1.[NH:17]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[C@@H:18]([C:22](O)=[O:23])[CH:19]([CH3:21])[CH3:20].C1C=CC2N(O)N=NC=2C=1.C(N(CC)CC)C.C(Cl)CCl>ClCCl>[NH2:16][C:8]1([C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=2)[CH2:13][CH2:12][N:11]([C:22](=[O:23])[C@H:18]([NH:17][C:25](=[O:26])[O:27][C:28]([CH3:31])([CH3:30])[CH3:29])[CH:19]([CH3:21])[CH3:20])[CH2:10][C:9]1([CH3:14])[CH3:15]

Participants

7

Procedure

A mixture of 4-(4-chlorophenyl)-3,3-dimethylpiperidin-4-amine (488 mg, 2.044 mmol), Boc-D-Val-OH (444 mg, 2.044 mmol), HOBT (626 mg, 4.09 mmol), and triethylamine (1.140 mL, 8.18 mmol) in dichloromethane (5 mL) was treated with EDC (784 mg, 4.09 mmol), and the mixture was stirred overnight at room temperature. The mixture was concentrated in-vacuo, and the residue was taken up in ethyl acetate. The organic phase was washed 3× with WATER, 3× with sat. sodium carbonate, and 1× with sat sodium chloride, dried over sodium sulfate, and concentrated in-vacuo. The residue was purified over silica gel, eluting with ethyl acetate/hexanes (25%-50%-100% EtOAc) to yield the title compound (845 mg, 1.929 mmol, 94% yield) as a colorless glass. MS (ESI+)=438.36, M+.

Workup

  1. concentrationThe mixture was concentrated in-vacuo
  2. washThe organic phase was washed 3× with WATER, 3× with sat. sodium carbonate, and 1× with sat sodium chloride
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated in-vacuo
  5. customThe residue was purified over silica gel
  6. washeluting with ethyl acetate/hexanes (25%-50%-100% EtOAc)

Sources & evidence

ORD record
ord-2f313a721cbd4792abbc1d86b44acf97
Source dataset
uspto-grants-2009_10
Patent number
US07601844B2

Reaction notes

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