1-Bromohexane → HCID 136128406, compound
Reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].Cl.[CH3:9][N:10]1[C:19]2[NH:18][C:17]3[CH:20]=[C:21]([CH3:24])[CH:22]=[CH:23][C:16]=3[N:15]([C:25]([C:27]3[CH:43]=[CH:42][C:30]([CH2:31][NH:32][C:33](=[O:41])[CH2:34][CH:35]4[CH2:40][CH2:39][NH:38][CH2:37][CH2:36]4)=[C:29]([F:44])[CH:28]=3)=[O:26])[CH2:14][C:13]=2[CH:12]=[N:11]1>CN(C=O)C.C(N(CC)CC)C>[CH3:9][N:10]1[C:19]2[NH:18][C:17]3[CH:20]=[C:21]([CH3:24])[CH:22]=[CH:23][C:16]=3[N:15]([C:25]([C:27]3[CH:43]=[CH:42][C:30]([CH2:31][NH:32][C:33](=[O:41])[CH2:34][CH:35]4[CH2:40][CH2:39][N:38]([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7])[CH2:37][CH2:36]4)=[C:29]([F:44])[CH:28]=3)=[O:26])[CH2:14][C:13]=2[CH:12]=[N:11]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 1-bromohexane (0.83 mg, 0.005 mmol) in DMF (0.05 ml) was added to a solution of N-[4-(3,6-dimethyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-2-fluoro-benzyl]-2-piperidin-4-yl-acetamide hydrochloride (Compound number 1110) (2.82 mg, 0.005 mmol) in DMF (0.05 ml) and triethyl-amine (0.0021 ml). The mixture was stirred for 20 h at room temperature then solvents were removed in vacuo to yield the title compound. (ESI)+: [M+H]+=575.7
Workup
- customsolvents were removed in vacuo
Sources & evidence
- ORD record
- ord-5db54cf69b1349a08bad0632108919fc
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08202858B2
Reaction notes
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