Hydrochloric Acid → HCID 13015361, compound

HRID 1732471Notes

Reaction equation

HRID 1732471 reaction equation
[C:1]1([S:7][C:8]2[CH:13]=[CH:12][N:11]=[C:10](C(NN)=O)[CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[N:19]([O-])=O.[Na+].C1(C2C=CN=C(C(N=[N+]=[N-])=S)C=2)C=CC=CC=1.[N-]=[N+]=[N-]>C(O)(=O)C.O>[C:1]1([S:7][C:8]2[CH:13]=[CH:12][N:11]=[C:10]([NH2:19])[CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

8

Procedure

A solution of 4-phenylthiopicolinic acid hydrazide 2.3 g. (0.050 mole) in 4.3 ml. of concentrated hydrochloric acid and 25 ml. of water is cooled to 75° C. and a solution of 3.55 g. of sodium nitrite in 6 ml. of water is added. The solution is stirred at 0°-5° for 20 minutes after the addition is complete. The resultant suspension is extracted with methylene chloride and the combined extracts are dried over sodium sulfate and evaporated in vacuo to yield 12.7 gm. of crude 4-phenylthio picolinic acid azide. The azide is heated in 60 ml. of 50% aqueous acetic acid at steam bath temperature for 40 minutes. The suspension is filtered and the filtrate is made basic with 50% sodium hydroxide. The solids are collected by filtration, washed with water, dried and chromatographed on silica gel. Elution with ethyl acetate yields 4-phenylthio 2-amino pyridine, the structure of which is characterized analytically.

Workup

  1. additionafter the addition
  2. extractionThe resultant suspension is extracted with methylene chloride
  3. dry with materialthe combined extracts are dried over sodium sulfate
  4. customevaporated in vacuo
  5. customto yield 12.7 gm
  6. filtrationThe suspension is filtered
  7. filtrationThe solids are collected by filtration
  8. washwashed with water
  9. customdried
  10. customchromatographed on silica gel
  11. washElution with ethyl acetate

Sources & evidence

ORD record
ord-2701875afac24fb0b5243cec7eda0cc1
Source dataset
uspto-grants-1980_12
Patent number
US04237300

Reaction notes

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