Propylamine → 2-Amino-4-chloro-6-propylamino-s-triazine

HRID 530043Notes

Reaction equation

HRID 530043 reaction equation
[NH2:1][C:2]1[N:7]=[C:6](Cl)[N:5]=[C:4]([Cl:9])[N:3]=1.[CH2:10]([NH2:13])[CH2:11][CH3:12].[OH-].[Na+]>CC(C)=O>[NH2:1][C:2]1[N:3]=[C:4]([Cl:9])[N:5]=[C:6]([NH:13][CH2:10][CH2:11][CH3:12])[N:7]=1

Participants

5

Conditions

Temperature
50 °C

Procedure

6-Amino-2,4-dichloro-[1,3,5]triazine (XXXVII) (30.0 g, 187 mmol) was dissolved in acetone (100 mL) and poured into ice-water (100 mL) to form a very fine suspension. To this mixture, a solution of propan-1-amine (11.0 g, 187 mmol) in acetone (20 mL) was added at 0° C. To this reaction, 2 N NaOH (94 mL, 187 mmol) was added dropwise at a rate to keep the temperature between 0° C. and 5° C. The mixture was stirred for 30 min at ambient temperature and for an additional 60 min at 50° C. The mixture was concentrated and then the precipitate was filtered off and washed with water (3×100 mL). After drying over calcium chloride under high vacuum, 6-amino-2-chloro-4-n-propylamino-[1,3,5]triazine (XXXVIII) was isolated as a white powder (35 g, 100% yield). LCMS (ESI) m/z=188 (M+H)+.

Workup

  1. customto form a very fine suspension
  2. additionwas added dropwise at a rate
  3. customthe temperature between 0° C. and 5° C
  4. concentrationThe mixture was concentrated
  5. filtrationthe precipitate was filtered off
  6. washwashed with water (3×100 mL)
  7. dry with materialAfter drying over calcium chloride under high vacuum

Sources & evidence

ORD record
ord-98a64d7d57ae46538849f36f6f512a7a
Source dataset
uspto-grants-2016_05
Patent number
US09351972B2

Reaction notes

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