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4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt

CAS No.
86477-09-0
Chemical Name:
4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt
Synonyms
Ethyl 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-2-carboxylate;5,6-dihydro-4H-Pyrrolo[1,2-b]pyrazole-2-carboxylic acid ethyl ester;4H-Pyrrolo[1,2-b]pyrazole-2-carboxylic acid, 5,6-dihydro-, ethyl ester;4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt;4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt (1:1)
CBNumber:
CB02510280
Molecular Formula:
C9H12N2O2
Molecular Weight:
180.2
MDL Number:
MFCD11975789
MOL File:
86477-09-0.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:47

4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt Properties

Melting point 61-63 °C
Boiling point 320.0±30.0 °C(Predicted)
Density 1.29±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka 0.56±0.20(Predicted)
Appearance Light yellow to yellow Solid
InChI InChI=1S/C9H12N2O2/c1-2-13-9(12)8-6-7-4-3-5-11(7)10-8/h6H,2-5H2,1H3
InChIKey MGGGSJRWNQFCLE-UHFFFAOYSA-N
SMILES N1=C(C(OCC)=O)C=C2CCCN12

SAFETY

Risk and Safety Statements

HS Code  2933998090

4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Apolloscientific OR930225 Ethyl 5,6-dihydro-4h-pyrrolo[1,2-b]pyrazole-2-carboxylate >99% 86477-09-0 100mg $21 2026-06-04 Buy
Apolloscientific OR930225 Ethyl 5,6-dihydro-4h-pyrrolo[1,2-b]pyrazole-2-carboxylate >99% 86477-09-0 250mg $22 2026-06-04 Buy
Apolloscientific OR930225 Ethyl 5,6-dihydro-4h-pyrrolo[1,2-b]pyrazole-2-carboxylate >99% 86477-09-0 1g $82 2026-06-04 Buy
Apolloscientific OR930225 Ethyl 5,6-dihydro-4h-pyrrolo[1,2-b]pyrazole-2-carboxylate >99% 86477-09-0 5g $168 2026-06-04 Buy
Apolloscientific OR930225 Ethyl 5,6-dihydro-4h-pyrrolo[1,2-b]pyrazole-2-carboxylate >99% 86477-09-0 25g $697 2026-06-04 Buy
Product number Packaging Price Buy
OR930225 100mg $21 Buy
OR930225 250mg $22 Buy
OR930225 1g $82 Buy
OR930225 5g $168 Buy
OR930225 25g $697 Buy

4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt Chemical Properties, Uses, Production

Synthesis

3a,4,5,6-tetrahydro-3-oxo-3H-Pyrrolo[1,2-c][1,2,3]oxadiazol-7-
iuM inner salt

98262-66-9

Ethyl propiolate

623-47-2

4H-Pyrrolo [1,2-C][1,2,3] oxadiazol -7-ium, 5,6-Dihydro -3-Hydroxy -, inner Salt

86477-10-3

4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt

86477-09-0

A reaction was carried out with 3a,4,5,6-tetrahydro-3-oxo-3H-pyrrolo[1,2-c][1,2,3]oxadiazol-7-ium innerium salt (13.5 g, 0.107 mol, crude from Example 4) and ethyl propargylate (15.8 g, 16.3 ml, 0.16 mol) in anhydrous N,N-dimethylformamide (50 ml) under nitrogen The reaction was stirred under protection and heated to 120-122 °C for 12 hours. The course of the reaction was monitored by HPLC (using a Prodigy ODS3 4.6×150 mm column with 90:10 to 10:90 water/acetonitrile containing 0.02% trifluoroacetic acid as the mobile phase in a gradient elution for 10 min). Under these conditions, the retention time of ethyl 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-2-carboxylate (the more polar target isomer) was 2.6-2.7 min, whereas the retention time of ethyl 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-3-carboxylate (the less polar non-target isomer) was 2.8-2.9 min. The UV detector was set at 215 nm because the absorption difference between the two isomers is significant at 254 nm and the non-target isomer is almost undetectable. After completion of the reaction, the mixture was concentrated to a dark syrupy consistency using an oil pump vacuum at a bath temperature not exceeding 50 °C. The ratio of the two esters in the dark syrup was 2.13:1 in favor of the target product ethyl 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-2-carboxylate as determined by NMR. The dark syrup was diluted with toluene and up-sampled by washing with hexane to a silica gel column (500 mL) preloaded in hexane. The column was eluted first with hexane-ethyl acetate (4:1) followed by hexane-ethyl acetate (1:1). The elution process was monitored by HPLC (conditions as above). Fractions containing both esters were collected and separated again by column chromatography. Fractions containing only ethyl 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-2-carboxylate were combined and concentrated to give 11 g (57%) of the pure product in white crystalline form with a melting point of 35-37 °C. Similarly, 6.5 g (33.7%) of ethyl 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-3-carboxylate was obtained as white crystals with a melting point of 205 °C.

References

[1] Patent: US2004/242874, 2004, A1. Location in patent: Page 13-14
[2] Indian Journal of Chemistry - Section B Organic Chemistry Including Medicinal Chemistry, 1991, vol. 30, # 2, p. 169 - 175
[3] Patent: US2004/242874, 2004, A1. Location in patent: Page 12-13
[4] Patent: US2004/242874, 2004, A1. Location in patent: Page 13
[5] Organic Process Research and Development, 2006, vol. 10, # 4, p. 712 - 716

4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt Preparation Products And Raw materials

4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt Suppliers

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4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt Spectrum

4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt (1:1) 5,6-dihydro-4H-Pyrrolo[1,2-b]pyrazole-2-carboxylic acid ethyl ester Ethyl 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-2-carboxylate 4H-Pyrrolo [1,2-B] pyrazole -2-carboxylic acid , 5,6-dihydro -, Potassium Salt 4H-Pyrrolo[1,2-b]pyrazole-2-carboxylic acid, 5,6-dihydro-, ethyl ester 86477-09-0