1,2-Dichloroethane → HCID 66836412, compound

HRID 879236Notes

Reaction equation

HRID 879236 reaction equation
C(Cl)CCl.C(N(CC)CC)C.[C:12]1([CH2:22][OH:23])[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:15]=[CH:14][CH:13]=1.[C:24]([NH:31][C@H:32]([C:40](O)=[O:41])[CH2:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25]>CN(C1C=CN=CC=1)C.ClCCl>[C:12]1([CH2:22][O:23][C:40](=[O:41])[C@H:32]([CH2:33][C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[NH:31][C:24]([O:26][C:27]([CH3:30])([CH3:28])[CH3:29])=[O:25])[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:15]=[CH:14][CH:13]=1

Participants

7

Procedure

1192 mg (6.2 mmol) of EDC, 578 μl (4.1 mmol) of triethylamine, 345 mg (2.8 mmol) of DMAP, and 328 mg (2.1 mmol) of 1-naphthylmethanol were added at RT to a solution of 500 mg (1.89 mmol) of N-Boc-L-phenylalanine in 25 ml dichlormethane. The reaction composition was stirred overnight, then diluted with 50 ml Dichlormethane and successively washed in a solution of 10% of aqueous citric acid, water, and saturated saline. The organic phase was dried over magnesium sulphate and then evaporated, and the residue purified with preparative HPLC. The yield was 501 mg (66% o. th.) of the title compound.

Workup

  1. washsuccessively washed in a solution of 10% of aqueous citric acid, water, and saturated saline
  2. dry with materialThe organic phase was dried over magnesium sulphate
  3. customevaporated
  4. customthe residue purified with preparative HPLC

Sources & evidence

ORD record
ord-dc0f972bf92c4b038fd810f65d9fe3e9
Source dataset
uspto-grants-2015_03
Patent number
US08987209B2

Reaction notes

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