Ammonium Chloride → HCID 178443787, compound

HRID 275569Notes

Reaction equation

HRID 275569 reaction equation
[PH:1](=[O:4])([OH:3])[OH:2].[CH:5]([CH:8]([CH:36]([CH3:38])[CH3:37])[CH:9]1[O:35][CH:10]1[C:11]1[N:15]=[CH:14][N:13]([C:16]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[N:12]=1)([CH3:7])[CH3:6].[N-:39]=[N+:40]=[N-:41].[Na+].[Cl-].[NH4+]>CO.O>[PH:1](=[O:2])([OH:4])[OH:3].[CH:5]([CH:8]([CH:36]([CH3:38])[CH3:37])[CH:9]([OH:35])[CH:10]([N:39]=[N+:40]=[N-:41])[C:11]1[N:15]=[CH:14][N:13]([C:16]([C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[N:12]=1)([CH3:7])[CH3:6]

Participants

5

Procedure

A mixture of diisopropyl (2RS,3SR)-2,3-epoxy-3(1-trityl-1,2,4-triazol-3-yl)propane phosphonate (6.83 g prepared as described in Example 51), sodium azide (4.18 g), ammonium chloride (1.51 g) and methanol-water (8:1, 125 ml) was heated under reflux for six hours, then concentrated under reduced pressure. The residue was filtered through silica in chloroform, then chromatographed on silica, using ethyl acetate-ethanol (20:1) as eluant, to give diisopropyl (2RS,3RS)-3-azido-2-hydroxy-3(1-trityl-1,2,4-triazol-3-yl)propane phosphonate (5.22 g, m.p. 137°-139° C., after trituration with ether). IR (nujol): 3304, 2104 cm-1. NMR (CDCl3 : δ1.3(12H,m), 1.9-2.25(2H,m), 4.17(1H,d), 4.45(1H,m), 4.68(2H,m), 4.78(1H,d), 7.1-7.4(15H,m), 7.98(1H,s). 13C NMR confirmed the regiochemistry.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for six hours
  3. concentrationconcentrated under reduced pressure
  4. filtrationThe residue was filtered through silica in chloroform
  5. customchromatographed on silica

Sources & evidence

ORD record
ord-4786de7bbce54d2fb31eb632f858158c
Source dataset
uspto-grants-1995_02
Patent number
US05393732

Reaction notes

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