Water → HCID 15171354, compound

HRID 1614775Notes

Reaction equation

HRID 1614775 reaction equation
[C:1](Cl)(=[O:3])[CH3:2].[NH2:5][CH2:6][C:7]1[C:8]([CH3:52])=[N:9][C:10]([CH3:51])=[CH:11][C:12]=1[O:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=2[C:27]2[N:28]=[N:29][N:30]([C:32]([C:45]3[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=3)([C:39]3[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=3)[C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)[N:31]=2)=[CH:17][CH:16]=1.C(N(CC)CC)C.O>ClCCl>[C:1]([NH:5][CH2:6][C:7]1[C:8]([CH3:52])=[N:9][C:10]([CH3:51])=[CH:11][C:12]=1[O:13][CH2:14][C:15]1[CH:16]=[CH:17][C:18]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=2[C:27]2[N:28]=[N:29][N:30]([C:32]([C:39]3[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=3)([C:45]3[CH:46]=[CH:47][CH:48]=[CH:49][CH:50]=3)[C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)[N:31]=2)=[CH:19][CH:20]=1)(=[O:3])[CH3:2]

Participants

6

Procedure

(Example 49A): A solution of acetyl chloride (79 mg) in dichloromethane (1 ml) was added to a solution of 3-aminomethyl-2,6-dimethyl-4-[(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)biphenyl-4-yl)methoxy]pyridine (628 mg) and triethylamine (101 mg) in dichloromethane (15 ml). The solution was left to stand for 1 hour and then water (15 ml) was added. The organic phase was separated, washed with saturated sodium chloride solution (15 ml) and then dried (MgSO4). The solvent was removed by evaporatoion and the residue was purified by flash chromatography, eluting with methanol/dichloromethane (1:19 v/v) to give 3-acetamidomethyl-2,6-dimethyl-4-[(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)biphenyl-4-yl)methoxy]pyridine (594 mg), as a foam; NMR (CDCl3): 1.8(s,3H), 2.5(s,3H), 2.6(s,3H), 4.45(d,2H), 5.0(s,2H), 5.6(br t, 1H), 6.6(s,1H), 6.9-7.0(m, 6H), 7.25-7.6 (complex m,16H), 7.95(dd,1H).

Workup

  1. waitThe solution was left
  2. customThe organic phase was separated
  3. washwashed with saturated sodium chloride solution (15 ml)
  4. dry with materialdried (MgSO4)
  5. customThe solvent was removed by evaporatoion
  6. customthe residue was purified by flash chromatography
  7. washeluting with methanol/dichloromethane (1:19 v/v)

Sources & evidence

ORD record
ord-e9c1cb4849e94ceca5af0cf05a994141
Source dataset
uspto-grants-1993_03
Patent number
US05198439

Reaction notes

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