Dichloromethane → HCID 53653455, compound

HRID 724864Notes

Reaction equation

HRID 724864 reaction equation
[Cl:1][C:2]1[N:6]([CH2:7][O:8][CH:9]([CH2:19][O:20]CC2C=CC=CC=2)[CH2:10][O:11]CC2C=CC=CC=2)[C:5]2[C:28]([Cl:35])=[C:29]([Cl:34])[C:30]([Cl:33])=[C:31]([Cl:32])[C:4]=2[N:3]=1.B(Cl)(Cl)Cl.C(Cl)Cl>CO>[Cl:1][C:2]1[N:6]([CH2:7][O:8][CH:9]([CH2:19][OH:20])[CH2:10][OH:11])[C:5]2[C:28]([Cl:35])=[C:29]([Cl:34])[C:30]([Cl:33])=[C:31]([Cl:32])[C:4]=2[N:3]=1

Participants

5

Procedure

Compound 155 (0.52 g, 51%) was prepared from 154 (1.5 g, 2.6 mmole), BCl3 (5M solution in CH2Cl2, 14 mL), CH2Cl2 (30 mL) and MeOH (20 mL) by the method described for 166 which on recrystallization from EtOAC gave 155: m.p. 155°; 1H NMR (DMSO-d6): d 5.76 (s, 2 H, C-1'), 4.63 (t, 2 H, exchanges with D2O, 2×OH), 3.54-3.48 (m, 1 H, C-3'), 3.43-3.25 (m, 4 H, C-4' and 5'H). Anal. Calcd. for C11H9N2Cl5O3 : C, 33.46; H, 2.28; N, 7.09. Found: C, 33.60; H, 2;15; N, 6.91.

Workup

  1. customdescribed for 166 which on recrystallization from EtOAC
  2. customgave 155

Sources & evidence

ORD record
ord-8699bcce8173455aac2c43856b6c4939
Source dataset
uspto-grants-1998_01
Patent number
US05705490

Reaction notes

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