ChemicalBook--->CAS DataBase List--->78485-37-7

78485-37-7

78485-37-7 Structure

78485-37-7 Structure
IdentificationBack Directory
[Name]

Ethyl 2-chloro-6-benzothiazolecarboxylate
[CAS]

78485-37-7
[Synonyms]

Ethyl 2-chloro-6-benzothiazolecarboxylate
Ethyl2-chlorobenzo[d]thiazole-6-carboxylate
2-Chlorobenzothiazole-6-carboxylic acid ethyl ester
6-Benzothiazolecarboxylic acid, 2-chloro-, ethyl ester
2-chloro-1,3-benzothiazole-6-carboxylic acid ethyl ester
JR-14052, Ethyl 2-chlorobenzo[d]thiazole-6-carboxylate, 97%
[Molecular Formula]

C10H8ClNO2S
[MDL Number]

MFCD08443995
[MOL File]

78485-37-7.mol
[Molecular Weight]

241.69
Chemical PropertiesBack Directory
[Melting point ]

90-92°
[Boiling point ]

340.5±15.0 °C(Predicted)
[density ]

1.400
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-1.37±0.10(Predicted)
[Appearance]

White to yellow Solid
[InChI]

InChI=1S/C10H8ClNO2S/c1-2-14-9(13)6-3-4-7-8(5-6)15-10(11)12-7/h3-5H,2H2,1H3
[InChIKey]

XISSCVMIXDMKLH-UHFFFAOYSA-N
[SMILES]

S1C2=CC(C(OCC)=O)=CC=C2N=C1Cl
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

2934208090
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 2-chloro-6-benzothiazolecarboxylate(78485-37-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethyl 2-amino-1,3-benzothiazole-6-carboxylate

50850-93-6

Ethyl 2-chloro-6-benzothiazolecarboxylate

78485-37-7

General procedure for the synthesis of ethyl 2-chlorobenzo[d]thiazole-6-carboxylate from ethyl 2-aminobenzo[d]thiazole-6-carboxylate: In a 500 mL single-necked flask, copper chloride (6.0 g, 44.6 mmol), tert-butyl nitrite (7.1 mL, 59.4 mmol), and acetonitrile (200 mL) were added and the mixture was cooled to 0 °C. Subsequently, ethyl 2-aminobenzo[d]thiazole-6-carboxylate (6.6 g, 29.7 mmol) was added in batches over 30 min. The reaction mixture was gradually warmed to room temperature and stirred overnight. After completion of the reaction, the filtrate was filtered through silica gel and the filtrate was added dropwise to 1 M HCl (60 mL) and stirred for 10 min to form a partition. The aqueous layer was extracted with ethyl acetate (100 mL), the organic layers were combined, washed with saturated brine and dried over anhydrous Na2SO4. After filtration again, it was rotary evaporated to dryness and purified by column chromatography (petroleum ether:ethyl acetate = 25:1) to afford 6.2 g of a pale yellow solid, ethyl 2-chlorobenzo[d]thiazole-6-carboxylate, in 86% yield. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 8.54 (d, J = 0.8 Hz, 1H), 8.20 (dd, J = 1.6 Hz, 8.4 Hz, 1H), 8.01 (d, J = 8.0 Hz, 1H), 4.45 (q, J = 7.2 Hz, 2H), 1.45 (t, J = 7.2 Hz, 3H).

[References]

[1] Patent: EP3401315, 2018, A1. Location in patent: Paragraph 0062; 0064
[2] Farmaco, 1994, vol. 49, # 3, p. 153 - 166
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