Haematopodin

Haematopodin is the more stable breakdown product of Haematopodin B.[1] Both compounds are found in the mushroom Mycena haematopus, although haematopodin only occurs in trace amounts in fresh fruit bodies. Similar pigments (with the 1,3,4,5-tetrahydropyrrolo[4,3,2-de]quinoline structure), known as batzellins and damirones, have been found in sea sponges.[1] A chemical synthesis for haematopodin was reported in 1996. Key steps in the synthesis involved the addition of 3-[(2,4-dimethoxybenzyl)amino]-1-propanol to the indolo-6,7-quinone and cyclization of the resulting adduct with trifluoroacetic acid.[2]

Haematopodin

Names
IUPAC name 6-oxa-2,11-diazatetracyclo[7.6.1.0^2,7.0^12,16]hexadeca-1(15),9,12(16)-triene-13,14-dione
Identifiers
CAS Number	151964-21-5
3D model (JSmol)	Interactive image
ChemSpider	10473906^Y
PubChem CID	10857709
InChI InChI=1S/C13H12N2O3/c16-9-5-8-11-7(6-14-12(11)13(9)17)4-10-15(8)2-1-3-18-10/h5-6,10,14H,1-4H2/t10-/m1/s1^Y Key: GTVMGUBGOSWMOJ-SNVBAGLBSA-N^Y InChI=1/C13H12N2O3/c16-9-5-8-11-7(6-14-12(11)13(9)17)4-10-15(8)2-1-3-18-10/h5-6,10,14H,1-4H2/t10-/m1/s1 Key: GTVMGUBGOSWMOJ-SNVBAGLBBX
SMILES O=C3/C=C2/N4CCCO[C@@H]4Cc1c[nH]c(c12)C3=O
Properties
Chemical formula	C13H12N2O3
Molar mass	244.250 g·mol^−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is ^YN ?)
Infobox references

References

1. Baumann, C.; Bröckelmann, M.; Fugmann, B.; Steglich, W.; Sheldrick, W. S. (1993). "Pigments of fungi. 62. Haematopodin, an unusual pyrrologuinone derivative isolated from the fungus Mycena haematopus, Agaricales". Angewandte Chemie International Edition in English. 32 (7): 1087–89. doi:10.1002/anie.199310871.
2. Hopmann, C.; Steglish, W. (1996). "Synthesis of haematopodin – A pigment from the mushroom Mycena haematopus (Basidiomycetes)". Liebigs Annalen. 1996 (7): 1117–20. doi:10.1002/jlac.15719960710.