Triethylamine → HCID 22000420, compound

HRID 1976122Notes

Reaction equation

HRID 1976122 reaction equation
[F:1][C:2]1[CH:16]=[CH:15][C:5]2[CH2:6][CH2:7][CH2:8][C:9]3[S:13][C:12]([NH2:14])=[N:11][C:10]=3[C:4]=2[CH:3]=1.C(N(CC)CC)C.[Br:24][CH2:25][CH2:26][CH2:27][CH2:28][C:29](Cl)=[O:30]>C1COCC1.CN(C1C=CN=CC=1)C>[F:1][C:2]1[CH:16]=[CH:15][C:5]2[CH2:6][CH2:7][CH2:8][C:9]3[S:13][C:12]([NH:14][C:29](=[O:30])[CH2:28][CH2:27][CH2:26][CH2:25][Br:24])=[N:11][C:10]=3[C:4]=2[CH:3]=1

Participants

6

Reactant 3

HCID 8471TriethylamineHCID 5211735-Bromovaleryl chloride2×HCID 11637238HCID 11637238, compound

Product 1

HCID 22000420HCID 22000420, compoundYield 70.4%

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 8028TetrahydrofuranSolvent

Procedure

9-Fluoro-5,6-dihydro-4H-benzo[6,7]cyclohepta[d][1,3]thiazol-2-amine (150 mg, 0.640 mmole) was dissolved in 3 ml of dry THF, mixed with triethylamine (135 μl, 0.970 mmole), cooled in an ice bath and treated with 5-bromovaleryl chloride (90 μl, 0.67 mmole). The mixture was stirred at room temperature for 3 days. TLC analysis of the mixture showed 50% completion. Hence, a catalytic amount of DMAP was added and stirring was continued for 16 hours. There was no change in the TLC of the mixture. 5-Bromovaleryl chloride (90 μl) was added and stirred for 3 days. The reaction mixture was partitioned between ethyl acetate and saturated sodium carbonate and the aqueous phase separated and extracted with 2×3 ml ethyl acetate. The combined ethyl acetate extracts were washed with saturated sodium chloride solution, concentrated and chromatographed (silica, Ethyl acetate/hexanes) to give 179 mg of the desired product as a white foam (70%): 397, 399 (ESMS, MH+).

Workup

  1. temperaturecooled in an ice bath
  2. stirringstirring
  3. waitwas continued for 16 hours
  4. stirringstirred for 3 days
  5. customThe reaction mixture was partitioned between ethyl acetate and saturated sodium carbonate
  6. customthe aqueous phase separated
  7. extractionextracted with 2×3 ml ethyl acetate
  8. washThe combined ethyl acetate extracts were washed with saturated sodium chloride solution
  9. concentrationconcentrated
  10. customchromatographed (silica, Ethyl acetate/hexanes)

Sources & evidence

ORD record
ord-1807e166dd0e44cb860252d4924419b8
Source dataset
uspto-grants-2001_05
Patent number
US06225330B1

Reaction notes

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