Basic information Safety Supplier Related

1-Chloro-5-isoquinolinesulfonyl Chloride

Basic information Safety Supplier Related

1-Chloro-5-isoquinolinesulfonyl Chloride Basic information

Product Name:
1-Chloro-5-isoquinolinesulfonyl Chloride
Synonyms:
  • 1-Chloro-5-isoquinolinesulfonyl Chloride
  • 1-Chloroisoquinoline-5-sulfonyl Chloride
  • 1-chloro-isoquinolin-5-sulfonyl chloride
  • 5-Isoquinolinesulfonyl chloride, 1-chloro-
CAS:
141519-77-9
MF:
C9H5Cl2NO2S
MW:
262.11
Product Categories:
  • Aromatics Compounds
  • Aromatics
  • Heterocycles
  • Sulfonyl Chlorides
Mol File:
141519-77-9.mol
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1-Chloro-5-isoquinolinesulfonyl Chloride Chemical Properties

Boiling point:
405.1±30.0 °C(Predicted)
Density 
1.584±0.06 g/cm3(Predicted)
storage temp. 
Storage temp. 2-8°C
solubility 
Chloroform, Dichloromethane
form 
Solid
pka
-0.24±0.43(Predicted)
color 
Off-White
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Safety Information

HS Code 
2933499090
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1-Chloro-5-isoquinolinesulfonyl Chloride Usage And Synthesis

Chemical Properties

Off-White Solid

Uses

1-Chloro-5-isoquinolinesulfonyl Chloride (cas# 141519-77-9) is a compound useful in organic synthesis.

Synthesis

7790-94-5

19493-44-8

141519-77-9

Chlorosulfonic acid (40 mL) was added slowly and dropwise to 1-chloroisoquinoline (9.92 g, 60.6 mmol) under nitrogen protection and at 0 °C under stirring. The reaction mixture was then heated at 155 °C for 24 hours. After completion of the reaction, the mixture was cooled to room temperature and slowly poured into ice (200 g). After cooling, the mixture was extracted with dichloromethane (300 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 13.6 g of 1-chloroisoquinoline-5-sulfonyl chloride as a white powder (51.9 mmol, 86% yield).1H NMR (CDCl3): δ 7.87 (t, J = 7.5 Hz, 1H), 8.52 (d, J = 6.2 Hz, 1H), 8.59 (d, J = 6.2 Hz, 1H ), 8.62 (d, J = 7.5 Hz, 1H), 8.82 (d, J = 7.5 Hz, 1H). Powdered 1-chloroisoquinoline-5-sulfonyl chloride (10.0 g, 38.2 mmol) was added batchwise to a stirred solution of tert-butyl (2-aminoethyl)-carbamate (7.33 g, 45.8 mmol) and triethylamine (10.7 mL, 76.4 mmol) in anhydrous dichloromethane (200 mL) at 0 °C. After the reaction mixture was stirred at room temperature for 4 h, it was concentrated and purified by silica gel column chromatography (elution gradient: dichloromethane solution in 0-5% methanol) to give 13.8 g of the product in foam form (35.8 mmol, 94% yield).ESIMS: m/z 386 [(M + H)+, 35Cl], 388 [(M + H)+, 37Cl]. Elemental analysis C16H20ClN3O4S: Calculated: C, 49.80; H, 5.22; N, 10.89; Measured: C, 49.70; H, 5.22; N, 10.72.

References

[1] Patent: WO2004/94386, 2004, A1. Location in patent: Page 27

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1-Chloro-5-isoquinolinesulfonyl Chloride(141519-77-9)Related Product Information