Sodium Sulfate → HCID 11589540, compound

HRID 1767032Notes

Reaction equation

HRID 1767032 reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([F:12])[CH:11]=1)[CH2:8][C:7](=O)[CH2:6][CH2:5]2.Cl.[CH:15]1([C:18]2[S:22][C:21]([NH:23][C:24](=[O:30])[CH:25]([NH2:29])[CH2:26][CH2:27][CH3:28])=[N:20][N:19]=2)[CH2:17][CH2:16]1.S([O-])([O-])(=O)=O.[Na+].[Na+].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl.C(O)(=O)C.C(N(CC)CC)C>[CH:15]1([C:18]2[S:22][C:21]([NH:23][C:24](=[O:30])[C@@H:25]([NH:29][CH:7]3[CH2:6][CH2:5][C:4]4[C:9](=[C:10]([F:12])[CH:11]=[C:2]([F:1])[CH:3]=4)[CH2:8]3)[CH2:26][CH2:27][CH3:28])=[N:20][N:19]=2)[CH2:16][CH2:17]1

Participants

8

Reactant 4

HCID 24436Sodium SulfateHCID 40764316,8-Difluoro-2-tetraloneHCID 5049666Sodium triacetoxyborohydrideHCID 131726497HCID 131726497, compound

Product 1

HCID 11589540HCID 11589540, compoundYield 75.3%

Reagents, catalysts & solvents 3

HCID 176Acetic AcidSolventHCID 6344DichloromethaneSolventHCID 8471TriethylamineSolvent

Procedure

A mixture of 6,8-difluoro-3,4-dihydro-1H-naphthalen-2-one (182 mg, 1.0 mmol), 2-amino-pentanoic acid (5-cyclopropyl-[1,3,4]thiadiazol-2-yl)-amide HCl (277 mg, 1.0 mmol) in methylene chloride (25 mL) was treated with triethyl amine (0.14 mL), then acetic acid (0.27 mL) and sodium sulfate. After stirring for 15 min, 95% pure sodium triacetoxy borohydride (424 mg, 2.0 mmol) was added and the resulting mixture was stirred at rt overnight. The mixture was quenched with dilute water and extracted with methylene chloride. The organic layer was washed with dilute sodium bicarbonate to pH 8, separated, dried and concentrated to give 306 mg of the title compound as a yellow glass foam, LC-MS, RT=1.9 min, M+1=407.0. The glass foam was purified by HPLC to give the trifluoroacetic acid salt of the title compound as a beige solid, LC-MS, RT=2.1 min, M+1=407.0.

Workup

  1. stirringthe resulting mixture was stirred at rt overnight
  2. customThe mixture was quenched with dilute water
  3. extractionextracted with methylene chloride
  4. washThe organic layer was washed with dilute sodium bicarbonate to pH 8
  5. customseparated
  6. customdried
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-dd919ef1a007419792240b8d1a92de41
Source dataset
uspto-grants-2007_06
Patent number
US07232820B2

Reaction notes

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