Thionyl Chloride → HCID 69878366, compound

HRID 1699676Notes

Reaction equation

HRID 1699676 reaction equation
[NH2:1][C:2]1[C:11]2[N:12]=[C:13]([CH2:22]O)[N:14]([CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1.S(Cl)([Cl:26])=O>>[ClH:26].[Cl:26][CH2:22][C:13]1[N:14]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:10]2[C:9]3[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=3[N:3]=[C:2]([NH2:1])[C:11]=2[N:12]=1

Participants

3

Reactant 2

HCID 24386Thionyl ChlorideHCID 9904568HCID 9904568, compound

Product 1

HCID 69878366HCID 69878366, compound

Procedure

4-Amino-1-phenylmethyl-1H-imidazo[4,5-c]-quinoline-2-methanol (2.0 g; 0.0066 mol, Example 27) was added in small portions to thionyl chloride (10 mL). After stirring at room temperature for 30 min the product had crystallized from solution. The mixture was diluted with dry ether (75 mL). The solid was filtered from the mixture, washed with ether, and thoroughly dried. The product was used as such without further characterization or purification.

Workup

  1. customhad crystallized from solution
  2. additionThe mixture was diluted with dry ether (75 mL)
  3. filtrationThe solid was filtered from the mixture
  4. washwashed with ether
  5. customthoroughly dried
  6. customsuch without further characterization or purification

Sources & evidence

ORD record
ord-8de35b5f3c23487ea36ee9b15f76d7f9
Source dataset
uspto-grants-2002_02
Patent number
US06348462B1

Reaction notes

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