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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965768Generated: October 30, 2026

HCID 59352086, compound → HCID 59352379, compound

https://huagongshe.com/reaction/1965768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59352086HCID 59352086—
ReactantHCID 59352535HCID 59352535—
ProductHCID 59352379HCID 59352379—

Reaction Steps

Following the procedure as described in EXAMPLE 13 and making non-critical variations using methyl 2-[(3-methyl-2′-oxospiro[furo[3,2-f][1,2]benzisoxazole-5,3′-indol]-1′(2′H)-yl)methyl]-1,3-oxazole-4-carboxylate to replace methyl 5-[(2′-oxo-5,6-dihydrospiro[benzo[1,2-b:5,4-b′]difuran-3,3′-indol]-1′(2′H)-yl)methyl]furan-2-carboxylate, 2-[(3-methyl-2′-oxospiro[furo[3,2-f][1,2]benzisoxazole-5,3′-indol]-1′(2′H)-yl)methyl]-1,3-oxazole-4-carboxylic acid was obtained (69%) as a colorless solid: 1H NMR (300 MHz, DMSO-d6) δ 13.13 (s, 1H), 8.70 (s, 1H), 7.74-7.71 (m, 1H), 7.40-7.34 (m, 1H), 7.26-7.23 (m, 2H), 7.07-7.02 (m, 2H), 5.28-5.22 (m, 2H), 5.00-4.90 (m, 2H), 2.39 (s, 3H); MS (ES+) m/z 417.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415370B2
Source datasetuspto-grants-2013_04
ORD IDord-1f6d535b55a44f9e9c5e9e954abba9c2
Source noteuspto-grants-2013_04