ChemicalBook--->CAS DataBase List--->105627-79-0

105627-79-0

105627-79-0 Structure

105627-79-0 Structure
IdentificationBack Directory
[Name]

Isoquinoline-5-sulphonyl chloride hydrochloride
[CAS]

105627-79-0
[Synonyms]

Isoquinoline-5-Sulphonyl
isoquinolin-5-sulfonyl chloride HCl
Isoquinolin-5-sulphonyl chloride HCl
Isoquinoline-5-sulphonyl chloride, HCl
5-(Chlorosulphonyl)isoquinoline hydrochloride
5-Isoquinolinesulfonyl chloride, hydrochloride
ISOQUINOLINE-5-SULPHONYL CHLORIDE HYDROCHLORIDE
isoquinolin-5-ylsulphonyl chloride hydrochloride
5-Isoquinolinesulfonylchloride, hydrochloride (1:1)
Isoquinoline-5-sulfonyl chloride hydrochloride salt
TIANFU-CHEM- Isoquinoline-5-sulphonyl chloride hydrochloride
5-(Chlorosulphonyl)isoquinoline hydrochloride, 5-(Chlorosulphonyl)-2-azanaphthalene hydrochloride
[EINECS(EC#)]

818-961-7
[Molecular Formula]

C9H7Cl2NO2S
[MDL Number]

MFCD08272853
[MOL File]

105627-79-0.mol
[Molecular Weight]

264.12
Chemical PropertiesBack Directory
[Melting point ]

173-183°C
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

DMSO (Sparingly, Heated)
[form ]

solid
[color ]

White
[Stability:]

Moisture Sensitive; Store in Freezer
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P280-P309+P311
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[HS Code ]

29334900
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

Isoquinoline-5-sulfonyl Chloride, Hydrochloride (cas# 105627-79-0) is a compound useful in organic synthesis.
[Synthesis]

5-Isoquinolinesulfonic acid

27655-40-9

Isoquinoline-5-sulphonyl chloride hydrochloride

105627-79-0

Anhydrous DMF (1.5 mL) was added slowly and dropwise to the suspension formed by stirring 5-isoquinolinesulfonic acid (28.3 g, 135 mmol) with thionyl chloride (150 mL, 2.06 mol) at room temperature and under nitrogen protection. The reaction mixture was heated to reflux and maintained for 2.5 hours. After completion of the reaction, it was cooled to room temperature and subsequently concentrated under reduced pressure to give a light yellow powder. The powder was suspended in anhydrous dichloromethane (200 mL), sonicated, filtered, and dried under reduced pressure at 40 °C to yield a final isoquinoline-5-sulfonyl chloride hydrochloride 29.2 g (111 mmol, 82% yield). The structure of the product was confirmed by 1H NMR (TFA-d): δ 8.48 (t, J = 7.9 Hz, 1H), 9.13-9.14 (m, 2H), 9.29 (d, J = 7.9 Hz, 1H), 9.57 (d, J = 7.0 Hz, 1H), 10.26 (s, 1H).

[References]

[1] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 9, p. 2317 - 2333
[2] Journal of Medicinal Chemistry, 1989, vol. 32, # 1, p. 42 - 46
[3] Journal of Medicinal Chemistry, 1989, vol. 32, # 1, p. 46 - 50
[4] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 9, p. 5277 - 5284
[5] Journal of Medicinal Chemistry, 2018, vol. 61, # 14, p. 5922 - 5933
Spectrum DetailBack Directory
[Spectrum Detail]

Isoquinoline-5-sulphonyl chloride hydrochloride(105627-79-0)1HNMR
Isoquinoline-5-sulphonyl chloride hydrochloride(105627-79-0)FT-IR
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