Acetic Acid → 7-Bromo-1,2,4,5-tetrahydro-pyrido[2,3-e][1,4]diazepin-3-one

HRID 2097107Notes

Reaction equation

HRID 2097107 reaction equation
[NH:1]1[C:7]2[N:8]=[CH:9][CH:10]=[CH:11][C:6]=2[CH2:5][NH:4][C:3](=[O:12])[CH2:2]1.C(O)(=O)C.[Br:17]Br>CCCCCC>[Br:17][C:10]1[CH:9]=[N:8][C:7]2[NH:1][CH2:2][C:3](=[O:12])[NH:4][CH2:5][C:6]=2[CH:11]=1

Participants

5

Reactant 3

HCID 176Acetic AcidHCID 24408BromineHCID 592775691H,2H,3H,4H,5H-pyrido[2,3-e][1,4]diazepin-3-one

Product 1

HCID 592776207-Bromo-1,2,4,5-tetrahydro-pyrido[2,3-e][1,4]diazepin-3-one

Reagents, catalysts & solvents 1

HCID 8058HexaneSolvent

Procedure

1,2,4,5-Tetrahydro-pyrido[2,3-e][1,4]diazepin-3-one (164 mg, 1.0 mmol) was dissolved into acetic acid (1 mL). Bromine (160 mg, 1.0 mmol) was added dropwise at room temperature and the solution was stirred overnight. Hexane (5 mL) was added and the orange precipitate was filtered and dried in vacuo. The title compound was isolated as an orange solid (190 mg, 78%). 1H NMR (300 MHz, DMSO-d6) δ 8.26 (t, J=5.7 Hz, 1H), 8.06 (d, J=2.1 Hz, 1H), 7.81 (d, J=2.1 Hz, 1H), 4.35 (d, J=5.7 Hz, 2H), 4.08 (s, 2H).

Workup

  1. filtrationthe orange precipitate was filtered
  2. customdried in vacuo

Sources & evidence

ORD record
ord-57fe8c1fda42440d85d65c635be9f383
Source dataset
uspto-grants-2013_05
Patent number
US08450307B2

Reaction notes

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