| Identification | More | [Name]
5-Chloroisatoic anhydride | [CAS]
4743-17-3 | [Synonyms]
5-CHLOROISATOIC ANHYDRIDE
5-CHLOROISATONIC ANHYDRIDE
6-CHLORO-1,2-DIHYDRO-4 H-3,1-BENZOXAZINE-2,4-DIONE
6-CHLORO-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE
6-chloro-4h-3,1-benzoxazine-2,4(1h)-dione
AKOS BBS-00002892
TIMTEC-BB SBB003570
5-Chloroisotoic anhydride
6-Chloro-2H-3,1-benzoxazine-2,4(1H)-dione
5-Chloroisatoic
5-Chloroisatoic anhydride 97%
5-Chloroisatoic anyhydride
1,4-Dihydro-6-chloro-2H-3,1-benzoxazine-2,4-dione
6-Chloro-1H-3,1-benzoxazine-2,4-dione
6-Chloro-4H-3,1-benzoxazine-2(1H),4-dione | [EINECS(EC#)]
225-255-7 | [Molecular Formula]
C8H4ClNO3 | [MDL Number]
MFCD00006701 | [Molecular Weight]
197.58 | [MOL File]
4743-17-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
300 °C (dec.) (lit.) | [density ]
1.540±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
DMSO (Slightly) | [form ]
Solid | [pka]
9.76±0.20(Predicted) | [color ]
Off-White | [InChI]
1S/C8H4ClNO3/c9-4-1-2-6-5(3-4)7(11)13-8(12)10-6/h1-3H,(H,10,12) | [InChIKey]
MYQFJMYJVJRSGP-UHFFFAOYSA-N | [SMILES]
Clc1ccc2NC(=O)OC(=O)c2c1 | [CAS DataBase Reference]
4743-17-3(CAS DataBase Reference) | [EPA Substance Registry System]
4743-17-3(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [TSCA ]
TSCA listed | [HS Code ]
2934999090 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
5-Chloroisatoic Anhydride was used as a reagent in the synthesis of 2-acetamidobenzamides bearing the 2-phenoxy functionality which display antiproliferative activity against certain tumor cell lines. Also used in the preparation of inhibitors of delta-5 desaturase. | [Preparation]
5-Chloroisatoic anhydride is prepared from 5-chloro indole (9c) by stirring in a 4:1 mixture of DMF/H2O for 16 h at room temperature.
1 H NMR (DMSO-d6): δ 11.85 (s, br., 1H), 7.96 (dd, J = 0.8, 8.7 Hz, 1H), 7.87 (dd, J = 2.3, 8.7 Hz, 1H), 7.09 (dd, J = 8.8, 0.8 Hz, 1H).
| [Synthesis]
Step 1 Synthesis of 6-chloro-1H-benzo[d][1,3]oxazine-2,4-dione: 2-Amino-5-chlorobenzoic acid (17 g, 0.1 mol) and 1,2-dichloroethane (200 mL) were added to a 500 mL three-necked round-bottom flask. A solution of triphosgene (21 g, 0.21 mol) in 1,2-dichloroethane (100 mL) was slowly added dropwise to the above solution at 80 °C. After the dropwise addition was completed, the reaction mixture was continued to be heated and stirred at 80°C for 3 hours. After completion of the reaction, the mixture was cooled to room temperature in an ice water bath. The precipitated white solid precipitate was collected by filtration and washed with an appropriate solvent and dried to afford 6-chloro-1H-benzo[d][1,3]oxazine-2,4-dione (19 g, 97% yield). The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 11.85 (br, 1H), 7.88 (d, J = 2.4 Hz, 1H), 7.78 (dd, J = 8.7, 2.4 Hz, 1H), 7.15 (d, J = 8.7 Hz, 1H). | [References]
[1] Patent: US2010/120741, 2010, A1. Location in patent: Page/Page column 78
[2] Patent: WO2011/112731, 2011, A2. Location in patent: Page/Page column 174
[3] Journal of Medicinal Chemistry, 2013, vol. 56, # 16, p. 6434 - 6456
[4] Chemical Biology and Drug Design, 2010, vol. 75, # 5, p. 444 - 454
[5] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 10, p. 2295 - 2299 |
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