Triethylamine → HCID 15016693, compound

HRID 1087602Notes

Reaction equation

HRID 1087602 reaction equation
[NH2:1][CH2:2][CH2:3][C@H:4]([OH:21])[C@@H:5]([NH:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:6][CH:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1.[CH3:22][CH:23]([CH3:28])[CH2:24][C:25](Cl)=[O:26].C(N(CC)CC)C>C(Cl)Cl>[CH3:22][CH:23]([CH3:28])[CH2:24][C:25]([NH:1][CH2:2][CH2:3][C@H:4]([OH:21])[C@@H:5]([NH:13][C:14]([O:16][C:17]([CH3:18])([CH3:20])[CH3:19])=[O:15])[CH2:6][CH:7]1[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12]1)=[O:26]

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 66054Isovaleryl chlorideHCID 15016692HCID 15016692, compound

Product 1

HCID 15016693HCID 15016693, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Conditions

Temperature
0 °C

Procedure

To (3S,4S)-1-amino-3-hydroxy-4-t-butyloxycarbonylamino-5-cyclohexylpentane (30.8 mg, 0.102 mmol) in dry methylene chloride (3 mL) at 0° C. was added 3-methyl-butyroyl chloride (0.123 mmol) and triethylamine (20.0 microliters, 0.143 mmol). The mixture was stirred at 0° C. for 1 hour, evaporated, taken up in methanol (3 mL) and treated with 1M NaOH (1 mL). After stirring for 1 hour, the mixture was diluted with ether, washed sequentially with 0.5M H3PO4, saturated NaHCO3 solution, and brine, and then dried over Na2SO4 and evaporated to afford the desired product.

Workup

  1. customevaporated
  2. additiontreated with 1M NaOH (1 mL)
  3. stirringAfter stirring for 1 hour
  4. additionthe mixture was diluted with ether
  5. washwashed sequentially with 0.5M H3PO4, saturated NaHCO3 solution, and brine
  6. dry with materialdried over Na2SO4
  7. customevaporated

Sources & evidence

ORD record
ord-438bd1a4fecc4f08ab8c73729b227914
Source dataset
uspto-grants-1991_07
Patent number
US05036051

Reaction notes

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