Acetic Acid → HCID 18784744, compound

HRID 1418727Notes

Reaction equation

HRID 1418727 reaction equation
[C:1]([C:9]1[CH:14]=[CH:13][C:12]([N:15]2[CH2:20][CH2:19][CH:18]([N:21]3[CH2:29][C:28]4[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=4)[C:22]3=[O:30])[CH2:17][CH2:16]2)=[CH:11][CH:10]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+].[C:33](O)(=O)[CH3:34].[CH3:37]O.[CH2:39]1[CH2:43]O[CH2:41][CH2:40]1>>[C:2]1([CH:1]([O:8][CH2:37][C:33]2[CH:34]=[CH:43][CH:39]=[CH:40][CH:41]=2)[C:9]2[CH:10]=[CH:11][C:12]([N:15]3[CH2:16][CH2:17][CH:18]([N:21]4[CH2:29][C:28]5[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=5)[C:22]4=[O:30])[CH2:19][CH2:20]3)=[CH:13][CH:14]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

5

Conditions

Temperature
0 °C

Procedure

To a solution of Example 280 compound (500 mg, 1.26 mmol) in MeOH/THF (1:1)(30 mL) at 0° C. was added sodium borohydride (48 mg, 1.26 mmol). The reaction was stirred at 0° C. for 2 hours then warmed to RT overnight. Acetic acid was added to quench the reaction until the reaction was pH 6 by pH paper. The resulting mixture was evaporated to dryness. Ethyl ether (200 mL) was added to the residue, and the organic layer was washed with water (2×50 mL), saturated sodium bicarbonate solution (2×50 mL), brine (2×50 mL) and dried over MgSO4. Evaporation gave title compound (355 mg, 71%) as a crude oil.

Workup

  1. temperaturethen warmed to RT overnight
  2. customto quench
  3. customthe reaction until the reaction
  4. customThe resulting mixture was evaporated to dryness
  5. additionEthyl ether (200 mL) was added to the residue
  6. washthe organic layer was washed with water (2×50 mL), saturated sodium bicarbonate solution (2×50 mL), brine (2×50 mL)
  7. dry with materialdried over MgSO4
  8. customEvaporation

Sources & evidence

ORD record
ord-f8273572c6034a4490ac509c3db74f55
Source dataset
uspto-grants-1999_03
Patent number
US05883099

Reaction notes

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